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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AL69
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 286 | 290 | PF00656 | 0.703 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.742 |
CLV_PCSK_FUR_1 | 37 | 41 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.664 |
CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 63 | 65 | PF00082 | 0.531 |
CLV_PCSK_PC7_1 | 35 | 41 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.487 |
DEG_COP1_1 | 130 | 140 | PF00400 | 0.566 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.662 |
DEG_SPOP_SBC_1 | 56 | 60 | PF00917 | 0.450 |
DOC_CKS1_1 | 264 | 269 | PF01111 | 0.370 |
DOC_CYCLIN_RxL_1 | 237 | 249 | PF00134 | 0.472 |
DOC_CYCLIN_RxL_1 | 434 | 444 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 147 | 155 | PF00069 | 0.348 |
DOC_MAPK_gen_1 | 184 | 190 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 237 | 246 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 255 | 264 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 62 | 69 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 148 | 157 | PF00069 | 0.338 |
DOC_MAPK_RevD_3 | 262 | 278 | PF00069 | 0.364 |
DOC_PP1_RVXF_1 | 240 | 247 | PF00149 | 0.453 |
DOC_PP1_RVXF_1 | 459 | 466 | PF00149 | 0.547 |
DOC_PP2B_LxvP_1 | 188 | 191 | PF13499 | 0.366 |
DOC_SPAK_OSR1_1 | 245 | 249 | PF12202 | 0.507 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.689 |
DOC_USP7_UBL2_3 | 233 | 237 | PF12436 | 0.484 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.688 |
DOC_USP7_UBL2_3 | 359 | 363 | PF12436 | 0.697 |
DOC_USP7_UBL2_3 | 420 | 424 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.602 |
LIG_14-3-3_CanoR_1 | 245 | 254 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.688 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.521 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.708 |
LIG_Integrin_RGD_1 | 284 | 286 | PF01839 | 0.577 |
LIG_LIR_Gen_1 | 427 | 432 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.458 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.353 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.545 |
LIG_SH3_4 | 359 | 366 | PF00018 | 0.614 |
LIG_Sin3_3 | 269 | 276 | PF02671 | 0.352 |
LIG_TRAF2_1 | 405 | 408 | PF00917 | 0.544 |
LIG_TRAF2_2 | 161 | 166 | PF00917 | 0.473 |
LIG_UBA3_1 | 234 | 242 | PF00899 | 0.412 |
MOD_CDC14_SPxK_1 | 110 | 113 | PF00782 | 0.457 |
MOD_CDC14_SPxK_1 | 94 | 97 | PF00782 | 0.592 |
MOD_CDK_SPK_2 | 307 | 312 | PF00069 | 0.765 |
MOD_CDK_SPK_2 | 347 | 352 | PF00069 | 0.548 |
MOD_CDK_SPxK_1 | 107 | 113 | PF00069 | 0.468 |
MOD_CDK_SPxK_1 | 91 | 97 | PF00069 | 0.600 |
MOD_CDK_SPxxK_3 | 107 | 114 | PF00069 | 0.480 |
MOD_CDK_SPxxK_3 | 307 | 314 | PF00069 | 0.659 |
MOD_CDK_SPxxK_3 | 91 | 98 | PF00069 | 0.601 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.595 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.599 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.656 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.516 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.680 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.707 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.797 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.489 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.453 |
MOD_Cter_Amidation | 336 | 339 | PF01082 | 0.501 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.684 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.601 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.821 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.638 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.584 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.326 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.723 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.726 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.633 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.717 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.665 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.548 |
MOD_NEK2_2 | 57 | 62 | PF00069 | 0.590 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.559 |
MOD_PKA_1 | 314 | 320 | PF00069 | 0.727 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.497 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.679 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.715 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.646 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.587 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.615 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.579 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.770 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.518 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.548 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.602 |
MOD_SUMO_rev_2 | 251 | 256 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 319 | 328 | PF00179 | 0.798 |
MOD_SUMO_rev_2 | 90 | 99 | PF00179 | 0.544 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.429 |
TRG_NLS_Bipartite_1 | 7 | 22 | PF00514 | 0.524 |
TRG_NLS_MonoExtC_3 | 313 | 318 | PF00514 | 0.762 |
TRG_NLS_MonoExtC_3 | 362 | 367 | PF00514 | 0.685 |
TRG_NLS_MonoExtN_4 | 311 | 318 | PF00514 | 0.722 |
TRG_NLS_MonoExtN_4 | 360 | 367 | PF00514 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 413 | 418 | PF00026 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 430 | 434 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB51 | Leptomonas seymouri | 61% | 100% |
A0A0S4IW25 | Bodo saltans | 30% | 100% |
A0A3R7ME95 | Trypanosoma rangeli | 40% | 100% |
A0A3S7WPV8 | Leishmania donovani | 88% | 100% |
A4H507 | Leishmania braziliensis | 72% | 99% |
A4HT71 | Leishmania infantum | 90% | 100% |
C9ZUP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 83% |
Q4QIN5 | Leishmania major | 89% | 99% |
V5BY30 | Trypanosoma cruzi | 41% | 98% |