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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9B5Q0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 141 | 145 | PF00656 | 0.300 |
CLV_C14_Caspase3-7 | 32 | 36 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.435 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.463 |
DEG_APCC_DBOX_1 | 112 | 120 | PF00400 | 0.541 |
DEG_MDM2_SWIB_1 | 72 | 80 | PF02201 | 0.273 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.377 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.373 |
DOC_CYCLIN_RxL_1 | 232 | 243 | PF00134 | 0.625 |
DOC_CYCLIN_yCln2_LP_2 | 343 | 349 | PF00134 | 0.634 |
DOC_CYCLIN_yCln2_LP_2 | 55 | 61 | PF00134 | 0.315 |
DOC_MAPK_gen_1 | 203 | 210 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 232 | 240 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 113 | 120 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 40 | 49 | PF00069 | 0.330 |
DOC_PP1_RVXF_1 | 234 | 241 | PF00149 | 0.545 |
DOC_PP1_RVXF_1 | 301 | 308 | PF00149 | 0.389 |
DOC_PP2B_LxvP_1 | 343 | 346 | PF13499 | 0.656 |
DOC_PP2B_LxvP_1 | 422 | 425 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.315 |
DOC_PP4_FxxP_1 | 188 | 191 | PF00568 | 0.500 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.393 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.621 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.541 |
LIG_Actin_WH2_2 | 167 | 184 | PF00022 | 0.450 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.273 |
LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.450 |
LIG_CaM_NSCaTE_8 | 76 | 83 | PF13499 | 0.429 |
LIG_Clathr_ClatBox_1 | 56 | 60 | PF01394 | 0.370 |
LIG_CSL_BTD_1 | 36 | 39 | PF09270 | 0.517 |
LIG_deltaCOP1_diTrp_1 | 71 | 76 | PF00928 | 0.322 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.182 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.501 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.442 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.478 |
LIG_GBD_Chelix_1 | 11 | 19 | PF00786 | 0.409 |
LIG_GBD_Chelix_1 | 408 | 416 | PF00786 | 0.256 |
LIG_LIR_Gen_1 | 106 | 117 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 162 | 172 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 370 | 380 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 423 | 434 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.351 |
LIG_NRBOX | 286 | 292 | PF00104 | 0.373 |
LIG_PCNA_PIPBox_1 | 301 | 310 | PF02747 | 0.395 |
LIG_PCNA_yPIPBox_3 | 203 | 214 | PF02747 | 0.533 |
LIG_PCNA_yPIPBox_3 | 406 | 420 | PF02747 | 0.366 |
LIG_Pex14_1 | 165 | 169 | PF04695 | 0.315 |
LIG_Pex14_2 | 126 | 130 | PF04695 | 0.375 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.450 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.356 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.350 |
LIG_Pex14_2 | 93 | 97 | PF04695 | 0.375 |
LIG_Pex3_1 | 287 | 298 | PF04882 | 0.433 |
LIG_REV1ctd_RIR_1 | 185 | 190 | PF16727 | 0.534 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.429 |
LIG_SH2_CRK | 52 | 56 | PF00017 | 0.380 |
LIG_SH2_CRK | 84 | 88 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 414 | 418 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 84 | 88 | PF00017 | 0.412 |
LIG_SH2_STAT3 | 407 | 410 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.273 |
LIG_SH3_2 | 346 | 351 | PF14604 | 0.621 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.599 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.391 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.348 |
LIG_Sin3_3 | 13 | 20 | PF02671 | 0.450 |
LIG_SUMO_SIM_anti_2 | 115 | 120 | PF11976 | 0.383 |
LIG_SUMO_SIM_anti_2 | 364 | 370 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 364 | 370 | PF11976 | 0.374 |
LIG_SUMO_SIM_par_1 | 40 | 46 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 415 | 421 | PF11976 | 0.227 |
LIG_SUMO_SIM_par_1 | 57 | 62 | PF11976 | 0.357 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.518 |
LIG_TYR_ITIM | 412 | 417 | PF00017 | 0.312 |
LIG_UBA3_1 | 55 | 64 | PF00899 | 0.159 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.556 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.329 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.483 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.518 |
MOD_Cter_Amidation | 216 | 219 | PF01082 | 0.317 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.416 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.326 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.408 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.412 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.299 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.487 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.334 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.675 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.553 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.375 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.370 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.327 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.366 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.318 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.357 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.434 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.231 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.532 |
MOD_NEK2_2 | 262 | 267 | PF00069 | 0.421 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.553 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.556 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.619 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.541 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.593 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.356 |
MOD_PKB_1 | 190 | 198 | PF00069 | 0.505 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.352 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.357 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.514 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.383 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.389 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.392 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.509 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.285 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.354 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.434 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.541 |
MOD_SUMO_rev_2 | 243 | 251 | PF00179 | 0.594 |
TRG_DiLeu_BaEn_1 | 209 | 214 | PF01217 | 0.483 |
TRG_DiLeu_BaEn_1 | 443 | 448 | PF01217 | 0.604 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 218 | 223 | PF00026 | 0.297 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRR8 | Leptomonas seymouri | 23% | 94% |
A0A0N1I533 | Leptomonas seymouri | 65% | 100% |
A0A0S4IQ17 | Bodo saltans | 28% | 93% |
A0A0S4JTI8 | Bodo saltans | 32% | 87% |
A0A1X0NKT2 | Trypanosomatidae | 32% | 100% |
A0A1X0NM00 | Trypanosomatidae | 24% | 96% |
A0A3Q8IGK4 | Leishmania donovani | 22% | 93% |
A0A3S5H7Y2 | Leishmania donovani | 95% | 100% |
A0A422P212 | Trypanosoma rangeli | 26% | 94% |
A4HE60 | Leishmania braziliensis | 22% | 100% |
A4HM51 | Leishmania braziliensis | 84% | 100% |
A4I1F8 | Leishmania infantum | 22% | 93% |
A4IAR3 | Leishmania infantum | 95% | 100% |
C9ZK11 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 94% |
D0A2E9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 95% |
E9AEI9 | Leishmania major | 95% | 100% |
E9AXJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q0VGV9 | Xenopus tropicalis | 21% | 83% |
Q4Q9X7 | Leishmania major | 23% | 100% |
Q658I5 | Oryza sativa subsp. japonica | 23% | 88% |
Q7SYR6 | Xenopus laevis | 22% | 83% |
Q9M028 | Arabidopsis thaliana | 24% | 88% |
Q9SR93 | Arabidopsis thaliana | 24% | 88% |