Features and Secondary Structure |
| 1 . 10 . 20 . 30 . 40 . 50 . 60 . 70 . 80 . 90 . 100 . 110 . 120 . 130 . 140 . 150 . 160 . 170 . 180 . 190 . 200 . 210 . 220 . 230 . 240 . 250 . 260 . 270 . 280 . 290 . 300 . 310 . 320 . 330 . 340 . 350 . 360 . 370 . 380 . 390 . 400 . 410 . 420 . 430 . 440 . 450 . 460 . 470 . 480 . 490 . 500 . 510 . 520 . 530 . 540 . 550 . 560 . 570 . 580 . 590 . 600 . 610 . 620 . 630 . 640 . 650 . 660 . 670 . 680 . 690 . 700 . 710 . 720 . 730 . 740 . 750 . 760 . 770 . 780 . 790 . 800 . 810 . 820 . 830 . 840 . 850 . 860 . 870 . 880 . 890 . 900 . 910 . 920 . 930 . 940 . 950 . 960 . 970 . 980 . 990 . 1000 . 1010 . 1020 . 1030 . 1040 . 1050 . 1060 . 1070 . 1080 . 1090 . 1100 . 1110 . 1120 . 1130 . |
| MAKNKQSVFEEKNYTQTEPENIFGDLYDGKSTVEEDPNIKVAYDADGNGYYIAFNKETGVYYDPYGDTEYDISQLFDENGNPFVFDEKQEENDYLKYVGNPDYGSYDENGEWVWSGYFENDQWISTKESQPTDENYGFDSDLPPEVKQPESVEDNYGFDNDLPPEVKQPESVEDNYGFDNDLPPEVKQPESVVDQPSSDDYFAKQPTDENYGFDNDLPPEVKQPESVVDQPSSDDHFAKQPESTTDSYSFDSDLPQPTLDQPSLDDHVQYNFDHHEELKPVAEEQNNYQVGFDQVQANLDNNEEIQPTAEKKVTTDFESKQAQVVDSYQLPIDTDQQDQTTFSSSFETQPTVEQFDQVNSEVNDQFKPEITKEPVLESSFNKQDVVETSDLNSESNLYSENNKDATNNDSLNSEFIQLNSNSETASDDVHYESKSEPIHDYKFGSDLSQSNSNNSLESEPVKFNSETAPDAHFESQSEPVDQVQYDIYQNEELKPTLDQPSSDDYFAKQPTDENYGFDNDLPPEVKQPESVVDQPSSDDHFAKQPESTTDSYSFDSDLPQPTLDQPSLDDHVQYNFDHHEELKPVAEEQNNYQVGFDQVQANLDNNEEIQPTAEKEVTTDFESKQAQVVDSYQLPIDTDQQDQTTFSSSFETQPTVEQFDQVNSEVNDQFKPEITKEPVLESSFNKQDVVETSNYTNNLQKFDIQSDNKITITTKKSSPQIPTTLPISFVSNRIEYKPVETLALDNKESQQEQITINSITEDSKTLAKTLSVQLQQINSLNNQSIVTSESVRLDKKDDQLTINTVNSEDQQPKIEVFVKAKEPVEEHSITQNKQSVEDKSELDNFNKKSDLYKIISELKRGELNPTINFDAIFQMNDYQMSVKQSFIHLNDFVTNYKNQISERYLIIKKELQSELSRLIDQNENLNVQFNNAKNLTTLQKEEMIRSLASDFAIAYKPSNSYEQLQKSGEIMRHVQRAITENEKKIESIQGSLKQLKTVYNSCCETIMNNINKLDNTLRFAKKEKDPLLLSNFDSVTDNGLVEPNQLMDDLIDFSNTFDNISNEQLDDFIYENMDRNIDFEFEGFNNDFVDIDAKVMDSMSAFSVNDLDIETLVPDRTSNFSSLLDEDLFESSGDFSLDY |
tmhmm (0) | ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- |
low complexity (5%) | ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------XXXXXXXXXXXXXX------------------------------------------XXXXXXXXXXXXXXX----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------XXXXXXXXXXXXXXXXX---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------XXXXXXXXXXXXX------- |
coiled-coils (4%) | -------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------XXXXXXXXXXXXXXXXXXXXXXXXXXXX-------------------------------------------------------------------XXXXXXXXXXXXXXXXXXXXX-------------------------------------------------------------------------------------------------------------------- |
disordered (56%) | XXXXXX-XXXXX-----------------------------------------------------------------------X-XX----------------------------------------XXXXXXXXXXXXXXXXXXXXXXXXXXXXXX----------XX-------X---XXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXX-------XXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXX--------XXXXXXXXXXXXXXXXXX-----XXXXXXXXXXXXXXXXXX----------------------XXXXXXXXXX-----------------XXXXXXXXXXXXXXXXXXXXX------------------------------XXXXXXXXXXXXXXXX--------------------------------------------------------------------------------------------------------------------XXXXXXXXXXX-----------X--------------------------------------------------------------------------------------------------------------------------------------------------------X--X-X |
psipred | ----HHHHH---------HHHHHHHH------------EEEEE------EEEEE-----EEEE--------HHHHH-----------------HHHH-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------HHH---------HH-----------------------------------------------------------------------------------------------------------------------------------------------HH---HHHH-------------------HHHHHHHHHHH---------------------------------EEE----------------------HHHHHH------HHHHHHHHH---------HHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH-EEEEEE----HHHHH-----HHHHHH------HHHHHHHHHHHHH---EEE-----HHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH-----HHH-------------HHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH------------------------------------EE--------HHHHHHHHHHH--------- |
PSI-BLAST Sequence Hits (Top 20 by Identity) ALL DATA
|
TaxID |
Species |
Alignments |
PSI-Blast Data (alignment with lowest E value) |
E value |
Query Span |
Sbjct Span |
Bit Score |
Identity |
HSP Length |
Accession |
Description |
662945 | Mycoplasma genitalium M6320 | 1 (0.16%) | 0.0 | 1-1139 | 1-1139 | 713 | 100 | 1139 | ref|NP_072979.1| | HMW1 cytadherence accessory protein [Mycoplasma genitalium G... |
662946 | Mycoplasma genitalium M6282 | 1 (0.16%) | 0.0 | 1-1139 | 1-1139 | 712 | 100 | 1139 | ref|YP_006600343.1| | HMW1 cytadherence accessory protein [Mycoplasma genitalium M... |
2097 | Mycoplasma genitalium | 2 (0.31%) | 2E-93 | 659-1139 | 1-481 | 351 | 100 | 481 | ref|WP_009885890.1| | HMW1 cytadherence accessory protein, partial [Mycoplasma gen... |
1112856 | Mycoplasma pneumoniae 309 | 1 (0.16%) | 2E-68 | 285-1139 | 137-1018 | 268 | 25 | 883 | ref|YP_005175689.1| | cytadherence accessory protein HMW1 [Mycoplasma pneumoniae 3... |
722438 | Mycoplasma pneumoniae FH | 1 (0.16%) | 2E-68 | 285-1139 | 137-1018 | 268 | 25 | 883 | ref|YP_005881453.1| | cytadherence high molecular weight protein 1 [Mycoplasma pne... |
1238993 | Mycoplasma pneumoniae M129-B7 | 1 (0.16%) | 2E-68 | 261-1139 | 152-1018 | 268 | 24 | 882 | ref|NP_110135.1| | cytadherence accessory protein HMW1 [Mycoplasma pneumoniae M... |
412133 | Trichomonas vaginalis G3 | 19 (2.98%) | 2E-19 | 621-1063 | 130-582 | 105 | 20 | 464 | ref|XP_001301913.1| | hypothetical protein [Trichomonas vaginalis G3] gb|EAX88983.... |
7462 | Apis dorsata | 1 (0.16%) | 0.0 | 4-1009 | 3695-4786 | 659 | 19 | 1139 | ref|XP_006616365.1| | PREDICTED: uncharacterized protein LOC102671488 [Apis dorsat... |
203119 | Clostridium thermocellum ATCC 27405 | 1 (0.16%) | 3E-50 | 118-825 | 1389-2089 | 207 | 16 | 710 | ref|YP_001039467.1| | cellulosome anchoring protein cohesin subunit [Clostridium t... |
492476 | Clostridium thermocellum JW20 | 1 (0.16%) | 7E-39 | 118-732 | 979-1568 | 170 | 16 | 615 | ref|WP_003511551.1| | cellulosome anchoring protein cohesin region [Clostridium th... |
1515 | Clostridium thermocellum | 1 (0.16%) | 3E-46 | 118-784 | 783-1444 | 194 | 15 | 669 | emb|CAA47841.1| | S-layer protein [Clostridium thermocellum] |
637887 | Clostridium thermocellum DSM 1313 | 1 (0.16%) | 7E-42 | 143-786 | 766-1395 | 180 | 15 | 646 | ref|YP_005687159.1| | cellulosome anchoring protein cohesin subunit [Clostridium t... |
1159201 | Mycoplasma gallisepticum WI01_2001.043-13-2P | 1 (0.16%) | 1E-31 | 89-1123 | 897-1880 | 146 | 14 | 1051 | ref|YP_006581441.1| | cytadherence-associated protein [Mycoplasma gallisepticum VA... |
1159200 | Mycoplasma gallisepticum NY01_2001.047-5-1P | 1 (0.16%) | 1E-31 | 89-1123 | 897-1880 | 146 | 14 | 1051 | ref|YP_006583726.1| | cytadherence-associated protein [Mycoplasma gallisepticum NY... |
1159204 | Mycoplasma gallisepticum NC08_2008.031-4-3P | 1 (0.16%) | 2E-31 | 89-1123 | 894-1877 | 145 | 14 | 1051 | ref|YP_006586728.1| | cytadherence-associated protein [Mycoplasma gallisepticum NC... |
7460 | Apis mellifera | 1 (0.16%) | 1E-103 | 151-1009 | 3951-4851 | 383 | 13 | 924 | ref|XP_006561030.1| | PREDICTED: LOW QUALITY PROTEIN: uncharacterized protein LOC5... |
10090 | Mus musculus | 19 (2.98%) | 1E-42 | 228-851 | 546-1161 | 182 | 13 | 632 | ref|NP_035871.2| | zonadhesin precursor [Mus musculus] |
1159203 | Mycoplasma gallisepticum CA06_2006.052-5-2P | 1 (0.16%) | 7E-32 | 89-1123 | 897-1880 | 146 | 13 | 1051 | ref|YP_006585978.1| | cytadherence-associated protein [Mycoplasma gallisepticum CA... |
1159202 | Mycoplasma gallisepticum NC06_2006.080-5-2P | 1 (0.16%) | 2E-31 | 89-1123 | 897-1880 | 145 | 13 | 1051 | ref|YP_006585225.1| | cytadherence-associated protein [Mycoplasma gallisepticum NC... |
708616 | Mycoplasma gallisepticum str. F | 1 (0.16%) | 1E-26 | 89-1123 | 972-1941 | 129 | 13 | 1049 | ref|YP_005880532.1| | putative cytadherence-associated protein [Mycoplasma gallise... |