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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WTX4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.493 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.555 |
CLV_PCSK_FUR_1 | 163 | 167 | PF00082 | 0.425 |
CLV_PCSK_FUR_1 | 51 | 55 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.623 |
CLV_Separin_Metazoa | 108 | 112 | PF03568 | 0.529 |
DEG_APCC_DBOX_1 | 553 | 561 | PF00400 | 0.624 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.478 |
DEG_SPOP_SBC_1 | 274 | 278 | PF00917 | 0.573 |
DOC_ANK_TNKS_1 | 229 | 236 | PF00023 | 0.421 |
DOC_MAPK_gen_1 | 461 | 468 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 51 | 59 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 67 | 73 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 24 | 32 | PF00069 | 0.443 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.595 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.603 |
LIG_14-3-3_CanoR_1 | 136 | 141 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 280 | 288 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 341 | 350 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 397 | 406 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 430 | 438 | PF00244 | 0.470 |
LIG_Actin_WH2_2 | 196 | 214 | PF00022 | 0.461 |
LIG_BRCT_BRCA1_1 | 277 | 281 | PF00533 | 0.515 |
LIG_DLG_GKlike_1 | 136 | 144 | PF00625 | 0.479 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.509 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.621 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.425 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.585 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.437 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.466 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.563 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.484 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.549 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.461 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.482 |
LIG_LIR_Gen_1 | 535 | 545 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 535 | 540 | PF02991 | 0.514 |
LIG_NRBOX | 6 | 12 | PF00104 | 0.512 |
LIG_PCNA_yPIPBox_3 | 2 | 11 | PF02747 | 0.480 |
LIG_RPA_C_Fungi | 153 | 165 | PF08784 | 0.628 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.532 |
LIG_SH2_NCK_1 | 453 | 457 | PF00017 | 0.535 |
LIG_SH2_SRC | 453 | 456 | PF00017 | 0.554 |
LIG_SH2_SRC | 98 | 101 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.532 |
LIG_SUMO_SIM_anti_2 | 244 | 249 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.339 |
LIG_TRAF2_1 | 365 | 368 | PF00917 | 0.506 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.431 |
LIG_TRAF2_1 | 441 | 444 | PF00917 | 0.426 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.565 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.713 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.537 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.574 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.544 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.447 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.509 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.602 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.442 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.457 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.497 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.685 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.612 |
MOD_GlcNHglycan | 306 | 310 | PF01048 | 0.428 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.570 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.580 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.535 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.493 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.525 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.464 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.559 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.577 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.614 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.605 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.557 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.557 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.577 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.467 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.467 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.488 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.452 |
MOD_NEK2_2 | 275 | 280 | PF00069 | 0.645 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.527 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.415 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.531 |
MOD_PK_1 | 489 | 495 | PF00069 | 0.531 |
MOD_PKA_1 | 53 | 59 | PF00069 | 0.410 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.676 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.573 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.436 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.565 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.542 |
MOD_PKB_1 | 51 | 59 | PF00069 | 0.412 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.417 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.519 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.441 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.425 |
MOD_Plk_2-3 | 429 | 435 | PF00069 | 0.468 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.522 |
MOD_SUMO_rev_2 | 297 | 303 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 358 | 366 | PF00179 | 0.480 |
TRG_DiLeu_BaEn_3 | 226 | 232 | PF01217 | 0.550 |
TRG_DiLeu_BaEn_4 | 107 | 113 | PF01217 | 0.546 |
TRG_DiLeu_BaEn_4 | 47 | 53 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.564 |
TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 163 | 166 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.580 |
TRG_NES_CRM1_1 | 104 | 115 | PF08389 | 0.531 |
TRG_NLS_MonoExtC_3 | 163 | 169 | PF00514 | 0.428 |
TRG_NLS_MonoExtN_4 | 163 | 168 | PF00514 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 118 | 123 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 165 | 169 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 348 | 352 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBD3 | Leptomonas seymouri | 68% | 91% |
A0A0S4JEJ6 | Bodo saltans | 35% | 95% |
A0A1X0NNU4 | Trypanosomatidae | 40% | 98% |
A0A422MW68 | Trypanosoma rangeli | 39% | 98% |
A4H8I8 | Leishmania braziliensis | 83% | 100% |
A4HWW5 | Leishmania infantum | 99% | 100% |
C9ZPQ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AQM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QEV3 | Leishmania major | 93% | 100% |
V5AX96 | Trypanosoma cruzi | 40% | 98% |