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. | 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. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 7 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0008352 | katanin complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005856 | cytoskeleton | 5 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043228 | non-membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 6 |
GO:0005840 | ribosome | 5 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: A4IC06
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007019 | microtubule depolymerization | 5 | 1 |
GO:0009987 | cellular process | 1 | 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:0003824 | catalytic activity | 1 | 5 |
GO:0004609 | phosphatidylserine decarboxylase activity | 5 | 5 |
GO:0005488 | binding | 1 | 9 |
GO:0005515 | protein binding | 2 | 9 |
GO:0008017 | microtubule binding | 5 | 9 |
GO:0008092 | cytoskeletal protein binding | 3 | 9 |
GO:0015631 | tubulin binding | 4 | 9 |
GO:0016829 | lyase activity | 2 | 5 |
GO:0016830 | carbon-carbon lyase activity | 3 | 5 |
GO:0016831 | carboxy-lyase activity | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.415 |
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.528 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.280 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.768 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.492 |
CLV_Separin_Metazoa | 87 | 91 | PF03568 | 0.509 |
DEG_APCC_DBOX_1 | 575 | 583 | PF00400 | 0.486 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.534 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.427 |
DOC_CYCLIN_yCln2_LP_2 | 260 | 266 | PF00134 | 0.509 |
DOC_CYCLIN_yCln2_LP_2 | 53 | 59 | PF00134 | 0.477 |
DOC_MAPK_gen_1 | 22 | 29 | PF00069 | 0.494 |
DOC_MAPK_HePTP_8 | 495 | 507 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 22 | 29 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 498 | 507 | PF00069 | 0.575 |
DOC_PP2B_LxvP_1 | 260 | 263 | PF13499 | 0.507 |
DOC_PP4_MxPP_1 | 582 | 585 | PF00568 | 0.571 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.570 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.352 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 127 | 135 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 17 | 25 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 216 | 226 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 235 | 244 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.239 |
LIG_14-3-3_CanoR_1 | 385 | 395 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 429 | 435 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 529 | 538 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 94 | 103 | PF00244 | 0.533 |
LIG_Actin_WH2_2 | 500 | 515 | PF00022 | 0.536 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.334 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.671 |
LIG_BRCT_BRCA1_1 | 515 | 519 | PF00533 | 0.499 |
LIG_eIF4E_1 | 501 | 507 | PF01652 | 0.536 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.394 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.415 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.397 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.494 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.535 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.300 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.435 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.579 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.552 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.365 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.416 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.778 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.518 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.495 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.409 |
LIG_Integrin_isoDGR_2 | 150 | 152 | PF01839 | 0.415 |
LIG_LIR_Apic_2 | 535 | 541 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 12 | 20 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 192 | 202 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 488 | 497 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 461 | 465 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 488 | 492 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.511 |
LIG_LYPXL_S_1 | 38 | 42 | PF13949 | 0.523 |
LIG_LYPXL_yS_3 | 39 | 42 | PF13949 | 0.531 |
LIG_Pex14_2 | 213 | 217 | PF04695 | 0.427 |
LIG_Pex14_2 | 462 | 466 | PF04695 | 0.536 |
LIG_Rb_pABgroove_1 | 160 | 168 | PF01858 | 0.310 |
LIG_Rb_pABgroove_1 | 450 | 458 | PF01858 | 0.450 |
LIG_SH2_CRK | 15 | 19 | PF00017 | 0.461 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 15 | 19 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 166 | 170 | PF00017 | 0.367 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.478 |
LIG_SH2_SRC | 456 | 459 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.482 |
LIG_SH3_2 | 393 | 398 | PF14604 | 0.714 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.703 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.748 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.543 |
LIG_Sin3_3 | 575 | 582 | PF02671 | 0.575 |
LIG_SUMO_SIM_anti_2 | 467 | 473 | PF11976 | 0.575 |
LIG_SUMO_SIM_anti_2 | 488 | 494 | PF11976 | 0.493 |
LIG_SUMO_SIM_anti_2 | 502 | 508 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 202 | 209 | PF11976 | 0.498 |
LIG_TRAF2_1 | 302 | 305 | PF00917 | 0.740 |
LIG_TYR_ITIM | 193 | 198 | PF00017 | 0.467 |
LIG_UBA3_1 | 120 | 128 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 210 | 215 | PF05994 | 0.511 |
LIG_WRC_WIRS_1 | 486 | 491 | PF05994 | 0.519 |
LIG_WW_3 | 395 | 399 | PF00397 | 0.580 |
LIG_WW_3 | 584 | 588 | PF00397 | 0.733 |
MOD_CDC14_SPxK_1 | 357 | 360 | PF00782 | 0.783 |
MOD_CDK_SPxK_1 | 354 | 360 | PF00069 | 0.734 |
MOD_CDK_SPxxK_3 | 145 | 152 | PF00069 | 0.334 |
MOD_CDK_SPxxK_3 | 319 | 326 | PF00069 | 0.677 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.376 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.457 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.466 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.459 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.729 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.679 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.775 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.575 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.465 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.478 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.376 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.536 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.505 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.387 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.477 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.422 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.491 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.454 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.757 |
MOD_GlcNHglycan | 374 | 378 | PF01048 | 0.771 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.649 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.673 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.631 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.371 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.489 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.365 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.192 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.382 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.459 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.494 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.787 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.786 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.540 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.796 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.473 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.457 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.538 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.731 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.635 |
MOD_N-GLC_2 | 556 | 558 | PF02516 | 0.318 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.396 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.537 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.265 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.332 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.450 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.565 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.540 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.561 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.367 |
MOD_NEK2_2 | 292 | 297 | PF00069 | 0.579 |
MOD_NEK2_2 | 508 | 513 | PF00069 | 0.506 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.513 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.657 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.536 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.536 |
MOD_PK_1 | 32 | 38 | PF00069 | 0.460 |
MOD_PKA_1 | 127 | 133 | PF00069 | 0.334 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.401 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.411 |
MOD_PKA_2 | 530 | 536 | PF00069 | 0.582 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.422 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.464 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.434 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.667 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.503 |
MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.505 |
MOD_Plk_2-3 | 82 | 88 | PF00069 | 0.499 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.361 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.667 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.573 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.402 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.444 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.334 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.428 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.674 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.693 |
TRG_DiLeu_BaEn_1 | 502 | 507 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 500 | 505 | PF01217 | 0.575 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 528 | 531 | PF00400 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 438 | 443 | PF00026 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 453 | 457 | PF00026 | 0.302 |
TRG_Pf-PMV_PEXEL_1 | 480 | 484 | PF00026 | 0.375 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P963 | Leptomonas seymouri | 67% | 100% |
A0A1X0P573 | Trypanosomatidae | 40% | 100% |
A0A3S7XA71 | Leishmania donovani | 100% | 100% |
A4HND4 | Leishmania braziliensis | 86% | 100% |
C9ZYJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AFU4 | Leishmania major | 96% | 100% |
E9B6Z6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q9BVA0 | Homo sapiens | 23% | 90% |