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: E9ARJ0
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 | 158 | 162 | PF00656 | 0.481 |
CLV_C14_Caspase3-7 | 211 | 215 | PF00656 | 0.379 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.631 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 64 | 66 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.279 |
DEG_SCF_FBW7_2 | 135 | 142 | PF00400 | 0.467 |
DEG_SCF_FBW7_2 | 319 | 325 | PF00400 | 0.405 |
DEG_SPOP_SBC_1 | 437 | 441 | PF00917 | 0.775 |
DOC_CDC14_PxL_1 | 472 | 480 | PF14671 | 0.588 |
DOC_CKS1_1 | 136 | 141 | PF01111 | 0.467 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.403 |
DOC_CYCLIN_RxL_1 | 85 | 93 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 238 | 247 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 253 | 262 | PF00069 | 0.234 |
DOC_MAPK_HePTP_8 | 235 | 247 | PF00069 | 0.277 |
DOC_MAPK_HePTP_8 | 252 | 264 | PF00069 | 0.217 |
DOC_MAPK_MEF2A_6 | 238 | 247 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.217 |
DOC_PP2B_LxvP_1 | 285 | 288 | PF13499 | 0.298 |
DOC_PP4_FxxP_1 | 434 | 437 | PF00568 | 0.533 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.576 |
DOC_USP7_UBL2_3 | 150 | 154 | PF12436 | 0.488 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.773 |
LIG_14-3-3_CanoR_1 | 338 | 343 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 65 | 74 | PF00244 | 0.554 |
LIG_Actin_WH2_2 | 89 | 104 | PF00022 | 0.595 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.573 |
LIG_CAP-Gly_1 | 518 | 526 | PF01302 | 0.584 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.581 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.398 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.312 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.298 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.269 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.736 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.596 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.488 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.410 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.495 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.746 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.264 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.279 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.580 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.379 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.592 |
LIG_LIR_Apic_2 | 341 | 345 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 499 | 508 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 279 | 283 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 336 | 342 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.442 |
LIG_MYND_1 | 476 | 480 | PF01753 | 0.594 |
LIG_PDZ_Class_3 | 521 | 526 | PF00595 | 0.579 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.347 |
LIG_Pex14_2 | 324 | 328 | PF04695 | 0.442 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.434 |
LIG_SH3_1 | 342 | 348 | PF00018 | 0.370 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.410 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.332 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.338 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.578 |
LIG_SUMO_SIM_anti_2 | 69 | 76 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 206 | 212 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 56 | 62 | PF11976 | 0.564 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.433 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.555 |
LIG_TYR_ITIM | 78 | 83 | PF00017 | 0.492 |
LIG_WRC_WIRS_1 | 501 | 506 | PF05994 | 0.622 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.473 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.719 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.520 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.733 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.634 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.513 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.699 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.801 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.538 |
MOD_GlcNHglycan | 18 | 22 | PF01048 | 0.451 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.398 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.620 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.506 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.383 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.616 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.705 |
MOD_GlcNHglycan | 44 | 48 | PF01048 | 0.673 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.716 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.648 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.674 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.414 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.568 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.424 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.383 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.541 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.458 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.720 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.696 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.661 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.550 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.456 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.324 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.498 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.661 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.546 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.426 |
MOD_NEK2_2 | 231 | 236 | PF00069 | 0.264 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.502 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.414 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.324 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.512 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.714 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.496 |
MOD_Plk_2-3 | 214 | 220 | PF00069 | 0.264 |
MOD_Plk_2-3 | 424 | 430 | PF00069 | 0.742 |
MOD_Plk_2-3 | 500 | 506 | PF00069 | 0.726 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.384 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.257 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.264 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.444 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.464 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.420 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.399 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.775 |
MOD_SUMO_rev_2 | 296 | 303 | PF00179 | 0.324 |
TRG_DiLeu_BaEn_1 | 222 | 227 | PF01217 | 0.279 |
TRG_DiLeu_BaEn_1 | 330 | 335 | PF01217 | 0.352 |
TRG_DiLeu_BaEn_1 | 350 | 355 | PF01217 | 0.349 |
TRG_DiLeu_BaEn_2 | 231 | 237 | PF01217 | 0.279 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.599 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.264 |
TRG_NES_CRM1_1 | 91 | 105 | PF08389 | 0.338 |
TRG_NLS_MonoExtN_4 | 180 | 186 | PF00514 | 0.415 |
TRG_NLS_MonoExtN_4 | 455 | 461 | PF00514 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 11 | 15 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 88 | 93 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3Z4 | Leptomonas seymouri | 57% | 100% |
A0A0S4J201 | Bodo saltans | 48% | 100% |
A0A1X0P6T6 | Trypanosomatidae | 55% | 100% |
A0A3R7NEX5 | Trypanosoma rangeli | 52% | 100% |
A0A3S5H730 | Leishmania donovani | 90% | 100% |
A4H9G1 | Leishmania braziliensis | 79% | 99% |
A4HXS8 | Leishmania infantum | 90% | 100% |
D0A060 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
V5BRP2 | Trypanosoma cruzi | 51% | 100% |