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:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4H530
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.397 |
CLV_PCSK_FUR_1 | 292 | 296 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.415 |
DEG_SPOP_SBC_1 | 390 | 394 | PF00917 | 0.689 |
DOC_ANK_TNKS_1 | 110 | 117 | PF00023 | 0.443 |
DOC_MAPK_gen_1 | 346 | 352 | PF00069 | 0.622 |
DOC_PP4_FxxP_1 | 337 | 340 | PF00568 | 0.584 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.717 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.750 |
LIG_14-3-3_CanoR_1 | 16 | 25 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 191 | 201 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 72 | 76 | PF00244 | 0.229 |
LIG_14-3-3_CterR_2 | 435 | 439 | PF00244 | 0.718 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.347 |
LIG_BIR_III_4 | 62 | 66 | PF00653 | 0.215 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.481 |
LIG_BRCT_BRCA1_1 | 211 | 215 | PF00533 | 0.425 |
LIG_deltaCOP1_diTrp_1 | 224 | 231 | PF00928 | 0.566 |
LIG_EH_1 | 174 | 178 | PF12763 | 0.420 |
LIG_EH_1 | 180 | 184 | PF12763 | 0.395 |
LIG_EVH1_2 | 114 | 118 | PF00568 | 0.446 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.476 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.599 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.311 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.272 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 26 | 34 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 74 | 83 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.238 |
LIG_PTB_Apo_2 | 171 | 178 | PF02174 | 0.412 |
LIG_RPA_C_Fungi | 342 | 354 | PF08784 | 0.452 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.584 |
LIG_SH2_GRB2like | 159 | 162 | PF00017 | 0.608 |
LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.675 |
LIG_SH2_NCK_1 | 186 | 190 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 267 | 271 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 138 | 141 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 290 | 293 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.663 |
LIG_SH3_1 | 109 | 115 | PF00018 | 0.764 |
LIG_SH3_1 | 120 | 126 | PF00018 | 0.487 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.764 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.487 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.756 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.651 |
LIG_SUMO_SIM_anti_2 | 32 | 38 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 35 | 40 | PF11976 | 0.282 |
LIG_TRAF2_1 | 418 | 421 | PF00917 | 0.658 |
LIG_TYR_ITIM | 206 | 211 | PF00017 | 0.323 |
LIG_TYR_ITIM | 75 | 80 | PF00017 | 0.243 |
LIG_UBA3_1 | 430 | 436 | PF00899 | 0.609 |
MOD_CDK_SPK_2 | 279 | 284 | PF00069 | 0.406 |
MOD_CDK_SPxxK_3 | 279 | 286 | PF00069 | 0.635 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.679 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.313 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.678 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.644 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.557 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.285 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.423 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.663 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.658 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.256 |
MOD_Cter_Amidation | 21 | 24 | PF01082 | 0.539 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.609 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.619 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.649 |
MOD_GlcNHglycan | 331 | 335 | PF01048 | 0.571 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.610 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.430 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.373 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.548 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.465 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.471 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.768 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.537 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.638 |
MOD_LATS_1 | 164 | 170 | PF00433 | 0.633 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.672 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.495 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.351 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.477 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.453 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.565 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.648 |
MOD_PKA_1 | 23 | 29 | PF00069 | 0.471 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.361 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.446 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.588 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.262 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.249 |
MOD_PKB_1 | 191 | 199 | PF00069 | 0.417 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.455 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.657 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.325 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.299 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.279 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.746 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.581 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.638 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.715 |
MOD_SUMO_rev_2 | 38 | 48 | PF00179 | 0.285 |
MOD_SUMO_rev_2 | 87 | 93 | PF00179 | 0.502 |
TRG_DiLeu_BaEn_3 | 320 | 326 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.277 |
TRG_ER_diArg_1 | 108 | 110 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 256 | 259 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 292 | 295 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 352 | 355 | PF00400 | 0.576 |
TRG_NES_CRM1_1 | 29 | 42 | PF08389 | 0.371 |
TRG_NLS_MonoExtC_3 | 48 | 53 | PF00514 | 0.334 |
TRG_NLS_MonoExtN_4 | 46 | 53 | PF00514 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYH8 | Leptomonas seymouri | 65% | 79% |
A0A0S4KL95 | Bodo saltans | 36% | 100% |
A0A1X0NR65 | Trypanosomatidae | 43% | 91% |
A0A3R7NAN2 | Trypanosoma rangeli | 44% | 88% |
A0A3S7WPX5 | Leishmania donovani | 75% | 100% |
A4HTA4 | Leishmania infantum | 78% | 78% |
C9ZUL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 90% |
E9AL93 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QIL1 | Leishmania major | 73% | 98% |
V5BTE7 | Trypanosoma cruzi | 44% | 84% |