A family of very long coiled-coil proteins, likely performing cytoskeletal functions.. Two varieties have evolved, one with an N-terminal FYVE domain (Non-TM) and another with a C-terminal PDZ domain (might be TM)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005576 | extracellular region | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0000795 | synaptonemal complex | 3 | 1 |
GO:0099086 | synaptonemal structure | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0006810 | transport | 3 | 5 |
GO:0006869 | lipid transport | 5 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0042157 | lipoprotein metabolic process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0051179 | localization | 1 | 5 |
GO:0051234 | establishment of localization | 2 | 5 |
GO:0071702 | organic substance transport | 4 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007130 | synaptonemal complex assembly | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0070192 | chromosome organization involved in meiotic cell cycle | 3 | 1 |
GO:0070193 | synaptonemal complex organization | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 5 |
GO:0008289 | lipid binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1180 | 1184 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.474 |
CLV_C14_Caspase3-7 | 954 | 958 | PF00656 | 0.506 |
CLV_NRD_NRD_1 | 1122 | 1124 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 1356 | 1358 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 816 | 818 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 887 | 889 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 960 | 962 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 1122 | 1124 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 1356 | 1358 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 816 | 818 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 887 | 889 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 940 | 942 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 960 | 962 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 940 | 942 | PF00082 | 0.416 |
CLV_PCSK_PC7_1 | 883 | 889 | PF00082 | 0.465 |
CLV_PCSK_PC7_1 | 956 | 962 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 1143 | 1147 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 1276 | 1280 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 1323 | 1327 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.473 |
CLV_Separin_Metazoa | 1234 | 1238 | PF03568 | 0.605 |
DEG_APCC_DBOX_1 | 1322 | 1330 | PF00400 | 0.495 |
DEG_SCF_FBW7_1 | 98 | 105 | PF00400 | 0.532 |
DEG_SCF_TRCP1_1 | 1180 | 1185 | PF00400 | 0.550 |
DOC_ANK_TNKS_1 | 698 | 705 | PF00023 | 0.272 |
DOC_CKS1_1 | 1187 | 1192 | PF01111 | 0.626 |
DOC_CKS1_1 | 119 | 124 | PF01111 | 0.630 |
DOC_CKS1_1 | 1308 | 1313 | PF01111 | 0.601 |
DOC_CYCLIN_yCln2_LP_2 | 1201 | 1207 | PF00134 | 0.533 |
DOC_MAPK_gen_1 | 1065 | 1073 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 1139 | 1148 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 1155 | 1164 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 1356 | 1364 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 841 | 848 | PF00069 | 0.415 |
DOC_MIT_MIM_1 | 859 | 867 | PF04212 | 0.486 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 1025 | 1029 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 1035 | 1039 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 1108 | 1112 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 1118 | 1122 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 1207 | 1211 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 1221 | 1225 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 1248 | 1252 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 767 | 771 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.436 |
DOC_USP7_UBL2_3 | 709 | 713 | PF12436 | 0.272 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 1186 | 1191 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 1196 | 1201 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 1226 | 1231 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 1307 | 1312 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.580 |
LIG_14-3-3_CanoR_1 | 1010 | 1019 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 1267 | 1275 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 1301 | 1308 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 916 | 926 | PF00244 | 0.421 |
LIG_Actin_WH2_2 | 995 | 1012 | PF00022 | 0.506 |
LIG_APCC_ABBA_1 | 672 | 677 | PF00400 | 0.272 |
LIG_APCC_ABBA_1 | 924 | 929 | PF00400 | 0.428 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.414 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.313 |
LIG_CtBP_PxDLS_1 | 1077 | 1083 | PF00389 | 0.438 |
LIG_eIF4E_1 | 1051 | 1057 | PF01652 | 0.507 |
LIG_FHA_1 | 1171 | 1177 | PF00498 | 0.483 |
LIG_FHA_1 | 1308 | 1314 | PF00498 | 0.738 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.393 |
LIG_FHA_1 | 720 | 726 | PF00498 | 0.444 |
LIG_FHA_1 | 802 | 808 | PF00498 | 0.440 |
LIG_FHA_2 | 1256 | 1262 | PF00498 | 0.582 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.570 |
LIG_FHA_2 | 788 | 794 | PF00498 | 0.452 |
LIG_FHA_2 | 941 | 947 | PF00498 | 0.487 |
LIG_LIR_Gen_1 | 1277 | 1284 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 1272 | 1278 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 1353 | 1358 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 31 | 35 | PF02991 | 0.313 |
LIG_PDZ_Class_1 | 1367 | 1372 | PF00595 | 0.327 |
LIG_RPA_C_Fungi | 1118 | 1130 | PF08784 | 0.498 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.327 |
LIG_SH2_SRC | 1280 | 1283 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 1215 | 1219 | PF00017 | 0.718 |
LIG_SH2_STAP1 | 1280 | 1284 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 1163 | 1166 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 1298 | 1301 | PF00017 | 0.675 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.491 |
LIG_SH3_1 | 104 | 110 | PF00018 | 0.595 |
LIG_SH3_2 | 1232 | 1237 | PF14604 | 0.607 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.627 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.646 |
LIG_SH3_3 | 1184 | 1190 | PF00018 | 0.611 |
LIG_SH3_3 | 1201 | 1207 | PF00018 | 0.509 |
LIG_SH3_3 | 1224 | 1230 | PF00018 | 0.636 |
LIG_SH3_3 | 1242 | 1248 | PF00018 | 0.542 |
LIG_SH3_3 | 1305 | 1311 | PF00018 | 0.587 |
LIG_SxIP_EBH_1 | 51 | 65 | PF03271 | 0.327 |
LIG_TRAF2_1 | 1328 | 1331 | PF00917 | 0.455 |
LIG_TRAF2_1 | 1346 | 1349 | PF00917 | 0.400 |
LIG_TRAF2_1 | 190 | 193 | PF00917 | 0.568 |
LIG_TRAF2_1 | 232 | 235 | PF00917 | 0.281 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.281 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.281 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.281 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.281 |
LIG_TRAF2_1 | 427 | 430 | PF00917 | 0.281 |
LIG_TRAF2_1 | 466 | 469 | PF00917 | 0.281 |
LIG_TRAF2_1 | 505 | 508 | PF00917 | 0.281 |
LIG_TRAF2_1 | 544 | 547 | PF00917 | 0.281 |
LIG_TRAF2_1 | 583 | 586 | PF00917 | 0.281 |
LIG_TRAF2_1 | 622 | 625 | PF00917 | 0.281 |
LIG_TRAF2_1 | 791 | 794 | PF00917 | 0.459 |
LIG_TRAF2_1 | 931 | 934 | PF00917 | 0.454 |
LIG_TRAF2_1 | 977 | 980 | PF00917 | 0.517 |
LIG_TYR_ITIM | 1278 | 1283 | PF00017 | 0.474 |
LIG_WW_3 | 1234 | 1238 | PF00397 | 0.605 |
MOD_CDK_SPK_2 | 1307 | 1312 | PF00069 | 0.598 |
MOD_CDK_SPxK_1 | 1196 | 1202 | PF00069 | 0.606 |
MOD_CDK_SPxK_1 | 98 | 104 | PF00069 | 0.588 |
MOD_CDK_SPxxK_3 | 1226 | 1233 | PF00069 | 0.645 |
MOD_CK1_1 | 1024 | 1030 | PF00069 | 0.597 |
MOD_CK1_1 | 1185 | 1191 | PF00069 | 0.601 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.498 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.558 |
MOD_CK1_1 | 951 | 957 | PF00069 | 0.471 |
MOD_CK2_1 | 1031 | 1037 | PF00069 | 0.516 |
MOD_CK2_1 | 1039 | 1045 | PF00069 | 0.524 |
MOD_CK2_1 | 1248 | 1254 | PF00069 | 0.615 |
MOD_CK2_1 | 1255 | 1261 | PF00069 | 0.567 |
MOD_CK2_1 | 1365 | 1371 | PF00069 | 0.331 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.572 |
MOD_CK2_1 | 787 | 793 | PF00069 | 0.449 |
MOD_CK2_1 | 940 | 946 | PF00069 | 0.484 |
MOD_GlcNHglycan | 1023 | 1026 | PF01048 | 0.649 |
MOD_GlcNHglycan | 1027 | 1030 | PF01048 | 0.569 |
MOD_GlcNHglycan | 1033 | 1036 | PF01048 | 0.554 |
MOD_GlcNHglycan | 1042 | 1045 | PF01048 | 0.539 |
MOD_GlcNHglycan | 1180 | 1183 | PF01048 | 0.556 |
MOD_GlcNHglycan | 1209 | 1212 | PF01048 | 0.497 |
MOD_GlcNHglycan | 1224 | 1227 | PF01048 | 0.592 |
MOD_GlcNHglycan | 1303 | 1306 | PF01048 | 0.586 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.615 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.449 |
MOD_GlcNHglycan | 919 | 922 | PF01048 | 0.402 |
MOD_GlcNHglycan | 963 | 966 | PF01048 | 0.497 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.539 |
MOD_GSK3_1 | 1010 | 1017 | PF00069 | 0.693 |
MOD_GSK3_1 | 1021 | 1028 | PF00069 | 0.544 |
MOD_GSK3_1 | 1031 | 1038 | PF00069 | 0.593 |
MOD_GSK3_1 | 1171 | 1178 | PF00069 | 0.489 |
MOD_GSK3_1 | 1182 | 1189 | PF00069 | 0.568 |
MOD_GSK3_1 | 1215 | 1222 | PF00069 | 0.598 |
MOD_GSK3_1 | 1313 | 1320 | PF00069 | 0.550 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.512 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.556 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.558 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.535 |
MOD_GSK3_1 | 961 | 968 | PF00069 | 0.494 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.569 |
MOD_NEK2_1 | 1021 | 1026 | PF00069 | 0.511 |
MOD_NEK2_1 | 1319 | 1324 | PF00069 | 0.629 |
MOD_NEK2_1 | 1333 | 1338 | PF00069 | 0.443 |
MOD_NEK2_1 | 1365 | 1370 | PF00069 | 0.332 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.596 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.329 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.444 |
MOD_NEK2_1 | 917 | 922 | PF00069 | 0.494 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.516 |
MOD_PIKK_1 | 1109 | 1115 | PF00454 | 0.525 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.682 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.332 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.281 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.281 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.281 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.281 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.281 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.281 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.297 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.281 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.281 |
MOD_PIKK_1 | 599 | 605 | PF00454 | 0.297 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.281 |
MOD_PKA_1 | 940 | 946 | PF00069 | 0.421 |
MOD_PKA_2 | 1021 | 1027 | PF00069 | 0.556 |
MOD_PKA_2 | 1266 | 1272 | PF00069 | 0.556 |
MOD_PKA_2 | 1300 | 1306 | PF00069 | 0.595 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.423 |
MOD_PKA_2 | 865 | 871 | PF00069 | 0.483 |
MOD_PKA_2 | 940 | 946 | PF00069 | 0.421 |
MOD_Plk_1 | 1182 | 1188 | PF00069 | 0.583 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.600 |
MOD_Plk_1 | 871 | 877 | PF00069 | 0.516 |
MOD_Plk_2-3 | 663 | 669 | PF00069 | 0.281 |
MOD_Plk_4 | 1015 | 1021 | PF00069 | 0.544 |
MOD_Plk_4 | 1171 | 1177 | PF00069 | 0.483 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.329 |
MOD_Plk_4 | 940 | 946 | PF00069 | 0.545 |
MOD_Plk_4 | 948 | 954 | PF00069 | 0.639 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.560 |
MOD_ProDKin_1 | 1186 | 1192 | PF00069 | 0.623 |
MOD_ProDKin_1 | 1196 | 1202 | PF00069 | 0.582 |
MOD_ProDKin_1 | 1226 | 1232 | PF00069 | 0.646 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.526 |
MOD_ProDKin_1 | 1307 | 1313 | PF00069 | 0.598 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.621 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.588 |
MOD_SUMO_rev_2 | 657 | 667 | PF00179 | 0.297 |
MOD_SUMO_rev_2 | 844 | 848 | PF00179 | 0.463 |
MOD_SUMO_rev_2 | 854 | 862 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_1 | 809 | 814 | PF01217 | 0.405 |
TRG_DiLeu_BaEn_4 | 192 | 198 | PF01217 | 0.622 |
TRG_DiLeu_BaLyEn_6 | 1069 | 1074 | PF01217 | 0.430 |
TRG_ENDOCYTIC_2 | 1275 | 1278 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 1280 | 1283 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 927 | 930 | PF00928 | 0.441 |
TRG_ER_diArg_1 | 1083 | 1086 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 1099 | 1102 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 1122 | 1124 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 1355 | 1357 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 887 | 889 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 913 | 916 | PF00400 | 0.500 |
TRG_NES_CRM1_1 | 838 | 851 | PF08389 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 1089 | 1093 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 1327 | 1331 | PF00026 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 928 | 933 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 972 | 976 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H530 | Leishmania donovani | 80% | 86% |
A4H3J9 | Leishmania braziliensis | 55% | 97% |
A4H3R9 | Leishmania braziliensis | 58% | 100% |