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: 10 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H9G1
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0034453 | microtubule anchoring | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005096 | GTPase activator activity | 4 | 11 |
GO:0008047 | enzyme activator activity | 3 | 11 |
GO:0030234 | enzyme regulator activity | 2 | 11 |
GO:0030695 | GTPase regulator activity | 4 | 11 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 11 |
GO:0098772 | molecular function regulator activity | 1 | 11 |
GO:0140677 | molecular function activator activity | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.379 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.309 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 182 | 184 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.191 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.448 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.594 |
DEG_SPOP_SBC_1 | 433 | 437 | PF00917 | 0.784 |
DOC_CYCLIN_RxL_1 | 85 | 93 | PF00134 | 0.579 |
DOC_MAPK_gen_1 | 237 | 246 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 252 | 261 | PF00069 | 0.234 |
DOC_MAPK_HePTP_8 | 234 | 246 | PF00069 | 0.277 |
DOC_MAPK_HePTP_8 | 251 | 263 | PF00069 | 0.217 |
DOC_MAPK_MEF2A_6 | 237 | 246 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 254 | 263 | PF00069 | 0.217 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.298 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.485 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.521 |
LIG_14-3-3_CanoR_1 | 337 | 342 | PF00244 | 0.519 |
LIG_Actin_WH2_2 | 89 | 104 | PF00022 | 0.587 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.561 |
LIG_CAP-Gly_1 | 516 | 522 | PF01302 | 0.592 |
LIG_DLG_GKlike_1 | 337 | 344 | PF00625 | 0.302 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.569 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.671 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.401 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.312 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.298 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.269 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.577 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.477 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.425 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.491 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.754 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.750 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.264 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.279 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.568 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.374 |
LIG_LIR_Gen_1 | 495 | 504 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 495 | 500 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.454 |
LIG_PDZ_Class_3 | 517 | 522 | PF00595 | 0.577 |
LIG_Pex14_2 | 176 | 180 | PF04695 | 0.352 |
LIG_Pex14_2 | 323 | 327 | PF04695 | 0.438 |
LIG_PTB_Apo_2 | 491 | 498 | PF02174 | 0.714 |
LIG_PTB_Phospho_1 | 491 | 497 | PF10480 | 0.714 |
LIG_SH2_NCK_1 | 449 | 453 | PF00017 | 0.517 |
LIG_SH2_SRC | 449 | 452 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.454 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.405 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.325 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.690 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.551 |
LIG_SUMO_SIM_anti_2 | 69 | 76 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 395 | 401 | PF11976 | 0.647 |
LIG_SUMO_SIM_par_1 | 56 | 62 | PF11976 | 0.547 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.654 |
LIG_TYR_ITIM | 78 | 83 | PF00017 | 0.508 |
LIG_WRC_WIRS_1 | 497 | 502 | PF05994 | 0.620 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.491 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.710 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.721 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.518 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.744 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.620 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.510 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.783 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.521 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.530 |
MOD_GlcNHglycan | 18 | 22 | PF01048 | 0.440 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.408 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.527 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.615 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.800 |
MOD_GlcNHglycan | 427 | 431 | PF01048 | 0.654 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.722 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.667 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.653 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.561 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.619 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.624 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.673 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.419 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.424 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.555 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.383 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.516 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.746 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.661 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.460 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.324 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.518 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.467 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.442 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.535 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.447 |
MOD_NEK2_2 | 230 | 235 | PF00069 | 0.264 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.498 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.470 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.422 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.324 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.526 |
MOD_Plk_1 | 495 | 501 | PF00069 | 0.711 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.508 |
MOD_Plk_2-3 | 152 | 158 | PF00069 | 0.505 |
MOD_Plk_2-3 | 213 | 219 | PF00069 | 0.264 |
MOD_Plk_2-3 | 421 | 427 | PF00069 | 0.742 |
MOD_Plk_2-3 | 496 | 502 | PF00069 | 0.723 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.388 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.667 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.264 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.456 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.721 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.417 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.576 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.521 |
MOD_SUMO_rev_2 | 295 | 302 | PF00179 | 0.324 |
TRG_DiLeu_BaEn_1 | 221 | 226 | PF01217 | 0.279 |
TRG_DiLeu_BaEn_1 | 349 | 354 | PF01217 | 0.344 |
TRG_DiLeu_BaEn_2 | 230 | 236 | PF01217 | 0.279 |
TRG_DiLeu_BaEn_4 | 351 | 357 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.599 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.624 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 251 | 254 | PF00400 | 0.264 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.313 |
TRG_NLS_MonoExtN_4 | 179 | 185 | PF00514 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 290 | 295 | PF00026 | 0.191 |
TRG_Pf-PMV_PEXEL_1 | 88 | 93 | PF00026 | 0.584 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3Z4 | Leptomonas seymouri | 68% | 100% |
A0A0S4J201 | Bodo saltans | 47% | 100% |
A0A1X0P6T6 | Trypanosomatidae | 53% | 100% |
A0A3R7NEX5 | Trypanosoma rangeli | 53% | 100% |
A0A3S5H730 | Leishmania donovani | 79% | 99% |
A4HXS8 | Leishmania infantum | 79% | 99% |
D0A060 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9ARJ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |
V5BRP2 | Trypanosoma cruzi | 50% | 100% |