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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X601
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.708 |
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 416 | 420 | PF00656 | 0.649 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.592 |
CLV_PCSK_FUR_1 | 329 | 333 | PF00082 | 0.586 |
CLV_PCSK_FUR_1 | 352 | 356 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 353 | 355 | PF00082 | 0.636 |
CLV_PCSK_PC7_1 | 327 | 333 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.408 |
DEG_APCC_DBOX_1 | 303 | 311 | PF00400 | 0.483 |
DEG_SPOP_SBC_1 | 362 | 366 | PF00917 | 0.650 |
DOC_ANK_TNKS_1 | 201 | 208 | PF00023 | 0.551 |
DOC_CKS1_1 | 347 | 352 | PF01111 | 0.474 |
DOC_PP1_RVXF_1 | 106 | 113 | PF00149 | 0.562 |
DOC_PP2B_PxIxI_1 | 43 | 49 | PF00149 | 0.421 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.476 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 304 | 308 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 334 | 343 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.675 |
LIG_Actin_WH2_2 | 21 | 38 | PF00022 | 0.292 |
LIG_APCC_ABBA_1 | 239 | 244 | PF00400 | 0.385 |
LIG_BIR_III_4 | 84 | 88 | PF00653 | 0.595 |
LIG_BRCT_BRCA1_1 | 193 | 197 | PF00533 | 0.605 |
LIG_eIF4E_1 | 15 | 21 | PF01652 | 0.400 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.531 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.663 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.530 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.624 |
LIG_GBD_Chelix_1 | 178 | 186 | PF00786 | 0.458 |
LIG_LIR_Gen_1 | 109 | 118 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 172 | 183 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 3 | 9 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.606 |
LIG_LYPXL_yS_3 | 79 | 82 | PF13949 | 0.622 |
LIG_NRBOX | 309 | 315 | PF00104 | 0.505 |
LIG_PDZ_Class_1 | 439 | 444 | PF00595 | 0.517 |
LIG_Pex14_2 | 112 | 116 | PF04695 | 0.594 |
LIG_SH2_PTP2 | 5 | 8 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.429 |
LIG_SH3_2 | 347 | 352 | PF14604 | 0.607 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.450 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.508 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.630 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.681 |
LIG_SUMO_SIM_par_1 | 289 | 296 | PF11976 | 0.462 |
LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.550 |
LIG_TRAF2_2 | 328 | 333 | PF00917 | 0.400 |
LIG_WW_3 | 231 | 235 | PF00397 | 0.656 |
MOD_CDK_SPxK_1 | 346 | 352 | PF00069 | 0.465 |
MOD_CDK_SPxxK_3 | 346 | 353 | PF00069 | 0.469 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.672 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.671 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.518 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.760 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.520 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.729 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.607 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.641 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.379 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.658 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.609 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.674 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.517 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.245 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.619 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.790 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.643 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.553 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.571 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.758 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.734 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.529 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.645 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.574 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.592 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.446 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.336 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.423 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.410 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.366 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.378 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.487 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.383 |
MOD_NEK2_2 | 303 | 308 | PF00069 | 0.452 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.575 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.563 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.472 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.687 |
MOD_PKB_1 | 332 | 340 | PF00069 | 0.573 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.689 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.536 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.664 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.506 |
MOD_Plk_2-3 | 419 | 425 | PF00069 | 0.611 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.481 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.375 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.454 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.570 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.573 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.547 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.727 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.515 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.699 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.691 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.465 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.674 |
MOD_SUMO_rev_2 | 238 | 248 | PF00179 | 0.396 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.648 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.580 |
TRG_NLS_MonoCore_2 | 351 | 356 | PF00514 | 0.576 |
TRG_NLS_MonoExtC_3 | 352 | 358 | PF00514 | 0.523 |
TRG_NLS_MonoExtN_4 | 350 | 357 | PF00514 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IME3 | Leptomonas seymouri | 53% | 100% |
A0A1X0NTD1 | Trypanosomatidae | 27% | 100% |
A0A422NZX0 | Trypanosoma rangeli | 29% | 100% |
A4HKT0 | Leishmania braziliensis | 79% | 99% |
A4I8A9 | Leishmania infantum | 99% | 100% |
D0AAI0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9B368 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
Q4Q4Y6 | Leishmania major | 89% | 100% |
V5DE70 | Trypanosoma cruzi | 29% | 100% |