Structural Proteins, Kinesin-like
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) | yes | yes: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
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. | yes | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 18 |
GO:0099080 | supramolecular complex | 2 | 18 |
GO:0099081 | supramolecular polymer | 3 | 18 |
GO:0099512 | supramolecular fiber | 4 | 18 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0097542 | ciliary tip | 2 | 1 |
Related structures:
AlphaFold database: A4I0Q2
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 18 |
GO:0007018 | microtubule-based movement | 3 | 18 |
GO:0009987 | cellular process | 1 | 18 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007019 | microtubule depolymerization | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 1 |
GO:0032984 | protein-containing complex disassembly | 5 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0051261 | protein depolymerization | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097435 | supramolecular fiber organization | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 18 |
GO:0003774 | cytoskeletal motor activity | 1 | 18 |
GO:0003777 | microtubule motor activity | 2 | 18 |
GO:0005488 | binding | 1 | 18 |
GO:0005515 | protein binding | 2 | 18 |
GO:0005524 | ATP binding | 5 | 18 |
GO:0008017 | microtubule binding | 5 | 18 |
GO:0008092 | cytoskeletal protein binding | 3 | 18 |
GO:0015631 | tubulin binding | 4 | 18 |
GO:0017076 | purine nucleotide binding | 4 | 18 |
GO:0030554 | adenyl nucleotide binding | 5 | 18 |
GO:0032553 | ribonucleotide binding | 3 | 18 |
GO:0032555 | purine ribonucleotide binding | 4 | 18 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 18 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 18 |
GO:0036094 | small molecule binding | 2 | 18 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043168 | anion binding | 3 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:0097367 | carbohydrate derivative binding | 2 | 18 |
GO:0140657 | ATP-dependent activity | 1 | 18 |
GO:1901265 | nucleoside phosphate binding | 3 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 522 | 526 | PF00656 | 0.449 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.365 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.512 |
CLV_Separin_Metazoa | 283 | 287 | PF03568 | 0.326 |
DEG_APCC_DBOX_1 | 66 | 74 | PF00400 | 0.434 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.536 |
DOC_CYCLIN_RxL_1 | 252 | 262 | PF00134 | 0.308 |
DOC_MAPK_gen_1 | 216 | 227 | PF00069 | 0.342 |
DOC_MAPK_HePTP_8 | 9 | 21 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 12 | 21 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 198 | 207 | PF00069 | 0.348 |
DOC_MAPK_RevD_3 | 124 | 137 | PF00069 | 0.346 |
DOC_PP1_RVXF_1 | 222 | 228 | PF00149 | 0.309 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.519 |
DOC_USP7_UBL2_3 | 491 | 495 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.131 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 224 | 228 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 294 | 298 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 316 | 324 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 46 | 52 | PF00244 | 0.305 |
LIG_Actin_WH2_2 | 273 | 288 | PF00022 | 0.312 |
LIG_APCC_ABBA_1 | 40 | 45 | PF00400 | 0.304 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.558 |
LIG_deltaCOP1_diTrp_1 | 365 | 370 | PF00928 | 0.495 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.308 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.308 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.329 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.534 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.308 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.398 |
LIG_LIR_Gen_1 | 173 | 183 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 226 | 231 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 48 | 55 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 95 | 99 | PF02991 | 0.358 |
LIG_NRP_CendR_1 | 576 | 577 | PF00754 | 0.643 |
LIG_Pex14_1 | 366 | 370 | PF04695 | 0.491 |
LIG_Pex14_2 | 51 | 55 | PF04695 | 0.388 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.398 |
LIG_SH2_NCK_1 | 108 | 112 | PF00017 | 0.326 |
LIG_SH2_SRC | 108 | 111 | PF00017 | 0.327 |
LIG_SH2_STAP1 | 108 | 112 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.386 |
LIG_SH3_2 | 347 | 352 | PF14604 | 0.641 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.500 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.252 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.735 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.516 |
LIG_SUMO_SIM_anti_2 | 18 | 24 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 256 | 262 | PF11976 | 0.308 |
LIG_TRAF2_1 | 520 | 523 | PF00917 | 0.568 |
LIG_TRFH_1 | 38 | 42 | PF08558 | 0.304 |
LIG_UBA3_1 | 138 | 146 | PF00899 | 0.275 |
LIG_UBA3_1 | 257 | 261 | PF00899 | 0.308 |
LIG_WRC_WIRS_1 | 127 | 132 | PF05994 | 0.317 |
LIG_WRC_WIRS_1 | 518 | 523 | PF05994 | 0.451 |
MOD_CDK_SPK_2 | 23 | 28 | PF00069 | 0.428 |
MOD_CDK_SPxxK_3 | 21 | 28 | PF00069 | 0.416 |
MOD_CDK_SPxxK_3 | 338 | 345 | PF00069 | 0.717 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.338 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.305 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.288 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.241 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.709 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.317 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.702 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.557 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.610 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.308 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.317 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.308 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.729 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.415 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.499 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.368 |
MOD_Cter_Amidation | 134 | 137 | PF01082 | 0.334 |
MOD_Cter_Amidation | 343 | 346 | PF01082 | 0.646 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.338 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.286 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.375 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.693 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.564 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.308 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.293 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.247 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.559 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.789 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.434 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.533 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.462 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.369 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.308 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.312 |
MOD_N-GLC_2 | 159 | 161 | PF02516 | 0.260 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.308 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.297 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.285 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.322 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.265 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.341 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.436 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.267 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.369 |
MOD_NEK2_2 | 80 | 85 | PF00069 | 0.308 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.353 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.231 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.317 |
MOD_PK_1 | 408 | 414 | PF00069 | 0.665 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.371 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.206 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.305 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.308 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.308 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.308 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.323 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.368 |
MOD_PKB_1 | 406 | 414 | PF00069 | 0.717 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.303 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.500 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.312 |
MOD_Plk_2-3 | 523 | 529 | PF00069 | 0.449 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.360 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.308 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.321 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.338 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.430 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.466 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.309 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.317 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.427 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.308 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.708 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.659 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.131 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.731 |
MOD_SUMO_for_1 | 333 | 336 | PF00179 | 0.636 |
MOD_SUMO_for_1 | 490 | 493 | PF00179 | 0.500 |
MOD_SUMO_for_1 | 511 | 514 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 238 | 246 | PF00179 | 0.312 |
MOD_SUMO_rev_2 | 487 | 497 | PF00179 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 68 | 73 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 405 | 408 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 533 | 536 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 12 | 16 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 136 | 140 | PF00026 | 0.331 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2G5 | Leptomonas seymouri | 81% | 100% |
A0A0N0P6P6 | Leptomonas seymouri | 42% | 87% |
A0A0N1PDD6 | Leptomonas seymouri | 30% | 76% |
A0A0S4IP49 | Bodo saltans | 27% | 72% |
A0A0S4IR67 | Bodo saltans | 29% | 74% |
A0A0S4IYW0 | Bodo saltans | 59% | 99% |
A0A1X0NIJ1 | Trypanosomatidae | 64% | 98% |
A0A1X0NQ03 | Trypanosomatidae | 26% | 70% |
A0A1X0NWZ8 | Trypanosomatidae | 30% | 77% |
A0A3R7MDH9 | Trypanosoma rangeli | 27% | 81% |
A0A3R7NVF2 | Trypanosoma rangeli | 65% | 100% |
A0A3S7WY84 | Leishmania donovani | 100% | 100% |
A0A3S7X9Y1 | Leishmania donovani | 31% | 100% |
A0A422MZ05 | Trypanosoma rangeli | 27% | 85% |
A0A422NEQ8 | Trypanosoma rangeli | 30% | 76% |
A0A422P4C5 | Trypanosoma rangeli | 39% | 80% |
A4HCT2 | Leishmania braziliensis | 32% | 80% |
A4HDC2 | Leishmania braziliensis | 92% | 100% |
A4HND6 | Leishmania braziliensis | 30% | 100% |
A4IC09 | Leishmania infantum | 31% | 100% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 77% |
C9ZXH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 84% |
D0A729 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
E9AFU7 | Leishmania major | 30% | 100% |
E9AJ89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 86% |
E9AWQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q4QAR9 | Leishmania major | 98% | 100% |
Q6P3R1 | Xenopus tropicalis | 28% | 90% |
Q7ZYL5 | Xenopus laevis | 30% | 89% |
Q940Y8 | Arabidopsis thaliana | 38% | 84% |
V5B8X9 | Trypanosoma cruzi | 27% | 82% |
V5BHI2 | Trypanosoma cruzi | 41% | 80% |
V5BK25 | Trypanosoma cruzi | 27% | 80% |
V5BLH7 | Trypanosoma cruzi | 30% | 67% |
V5D311 | Trypanosoma cruzi | 43% | 85% |
V5D733 | Trypanosoma cruzi | 30% | 77% |
V5DSJ9 | Trypanosoma cruzi | 67% | 100% |