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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005929 | cilium | 4 | 2 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
GO:0031514 | motile cilium | 5 | 1 |
Related structures:
AlphaFold database: A4HFX1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.581 |
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.573 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.779 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.651 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.804 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 290 | 292 | PF00082 | 0.698 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.558 |
CLV_PCSK_PC7_1 | 128 | 134 | PF00082 | 0.538 |
CLV_PCSK_PC7_1 | 414 | 420 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.565 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.556 |
DOC_PP2B_LxvP_1 | 59 | 62 | PF13499 | 0.569 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.778 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.651 |
DOC_USP7_UBL2_3 | 328 | 332 | PF12436 | 0.725 |
DOC_USP7_UBL2_3 | 348 | 352 | PF12436 | 0.733 |
DOC_USP7_UBL2_3 | 434 | 438 | PF12436 | 0.706 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 219 | 227 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 91 | 95 | PF00244 | 0.741 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.674 |
LIG_EVH1_2 | 338 | 342 | PF00568 | 0.560 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.579 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.595 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.755 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.579 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 71 | 82 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.556 |
LIG_SH2_PTP2 | 271 | 274 | PF00017 | 0.646 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.646 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.516 |
LIG_TYR_ITIM | 161 | 166 | PF00017 | 0.474 |
MOD_CDC14_SPxK_1 | 118 | 121 | PF00782 | 0.563 |
MOD_CDK_SPK_2 | 34 | 39 | PF00069 | 0.559 |
MOD_CDK_SPxK_1 | 115 | 121 | PF00069 | 0.566 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.738 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.576 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.575 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.692 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.736 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.630 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.755 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.738 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.597 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.690 |
MOD_Cter_Amidation | 126 | 129 | PF01082 | 0.690 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.684 |
MOD_GlcNHglycan | 23 | 27 | PF01048 | 0.680 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.512 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.746 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.730 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.628 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.598 |
MOD_GlcNHglycan | 84 | 88 | PF01048 | 0.601 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.742 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.574 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.609 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.577 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.649 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.615 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.612 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.714 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.646 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.677 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.616 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.657 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.653 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.803 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.697 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.672 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.573 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.578 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.735 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.578 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.546 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.564 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.578 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.635 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.562 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.574 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.739 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.685 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.472 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.558 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.566 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.732 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.726 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.539 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.575 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.679 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.646 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.556 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 77 | 80 | PF00400 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IE97 | Leishmania donovani | 60% | 100% |
A4I303 | Leishmania infantum | 60% | 100% |
E9ADH6 | Leishmania major | 60% | 98% |
E9AZA0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |