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:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HDN0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.513 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.721 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.411 |
CLV_PCSK_FUR_1 | 127 | 131 | PF00082 | 0.393 |
CLV_PCSK_FUR_1 | 143 | 147 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.342 |
DEG_APCC_DBOX_1 | 355 | 363 | PF00400 | 0.620 |
DEG_SPOP_SBC_1 | 284 | 288 | PF00917 | 0.446 |
DOC_CYCLIN_yCln2_LP_2 | 240 | 246 | PF00134 | 0.620 |
DOC_MAPK_MEF2A_6 | 238 | 247 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 302 | 311 | PF00069 | 0.515 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.694 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.690 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.573 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.609 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 174 | 182 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 238 | 243 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 369 | 377 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 458 | 468 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 64 | 72 | PF00244 | 0.677 |
LIG_Actin_WH2_2 | 300 | 317 | PF00022 | 0.555 |
LIG_AP2alpha_2 | 274 | 276 | PF02296 | 0.575 |
LIG_APCC_ABBA_1 | 273 | 278 | PF00400 | 0.585 |
LIG_CaM_IQ_9 | 119 | 135 | PF13499 | 0.637 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.626 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.559 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.551 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.197 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.622 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.533 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.658 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.577 |
LIG_LIR_Gen_1 | 241 | 251 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 328 | 334 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 53 | 59 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.646 |
LIG_Pex14_1 | 108 | 112 | PF04695 | 0.555 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.607 |
LIG_SH2_NCK_1 | 33 | 37 | PF00017 | 0.640 |
LIG_SH2_NCK_1 | 360 | 364 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.644 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.674 |
LIG_SH3_5 | 266 | 270 | PF00018 | 0.637 |
LIG_SUMO_SIM_par_1 | 424 | 431 | PF11976 | 0.583 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.608 |
LIG_TRFH_1 | 148 | 152 | PF08558 | 0.526 |
LIG_TRFH_1 | 271 | 275 | PF08558 | 0.531 |
LIG_TRFH_1 | 360 | 364 | PF08558 | 0.474 |
LIG_TYR_ITIM | 268 | 273 | PF00017 | 0.538 |
LIG_UBA3_1 | 353 | 358 | PF00899 | 0.498 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.510 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.426 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.531 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.517 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.621 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.545 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.596 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.623 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.652 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.506 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.468 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.538 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.615 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.557 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.318 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.495 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.322 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.297 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.566 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.640 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.299 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.367 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.575 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.662 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.516 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.313 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.466 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.563 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.454 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.334 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.318 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.287 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.358 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.240 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.418 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.686 |
MOD_PKA_1 | 369 | 375 | PF00069 | 0.302 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.682 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.754 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.637 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.421 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.642 |
MOD_PKB_1 | 175 | 183 | PF00069 | 0.572 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.279 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.321 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.426 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.283 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.311 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.568 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.521 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.746 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 149 | 154 | PF01217 | 0.364 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.589 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.670 |
TRG_ER_diArg_1 | 127 | 130 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.514 |
TRG_NLS_Bipartite_1 | 113 | 130 | PF00514 | 0.506 |
TRG_NLS_MonoExtC_3 | 125 | 130 | PF00514 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7U8 | Leptomonas seymouri | 62% | 99% |
A0A0S4JPE5 | Bodo saltans | 42% | 100% |
A0A1X0NW21 | Trypanosomatidae | 51% | 100% |
A0A3S7WYL2 | Leishmania donovani | 85% | 100% |
C9ZWD5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AH77 | Leishmania infantum | 85% | 100% |
E9AX15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QAG1 | Leishmania major | 84% | 100% |
V5DBL9 | Trypanosoma cruzi | 48% | 100% |