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 |
Related structures:
AlphaFold database: A4HLP2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 119 | 123 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.458 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.456 |
DEG_APCC_KENBOX_2 | 129 | 133 | PF00400 | 0.429 |
DOC_CKS1_1 | 287 | 292 | PF01111 | 0.563 |
DOC_CYCLIN_RxL_1 | 191 | 201 | PF00134 | 0.322 |
DOC_CYCLIN_RxL_1 | 278 | 291 | PF00134 | 0.534 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 130 | 138 | PF00134 | 0.386 |
DOC_MAPK_gen_1 | 212 | 222 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 237 | 244 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 95 | 103 | PF00069 | 0.531 |
DOC_PP2B_LxvP_1 | 367 | 370 | PF13499 | 0.475 |
DOC_PP4_FxxP_1 | 103 | 106 | PF00568 | 0.391 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 212 | 216 | PF12436 | 0.491 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.441 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 363 | 368 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 373 | 382 | PF00244 | 0.466 |
LIG_Actin_WH2_2 | 259 | 274 | PF00022 | 0.527 |
LIG_Actin_WH2_2 | 57 | 74 | PF00022 | 0.557 |
LIG_BIR_III_2 | 256 | 260 | PF00653 | 0.446 |
LIG_deltaCOP1_diTrp_1 | 405 | 410 | PF00928 | 0.418 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.452 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.550 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.328 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.641 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.488 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.387 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.389 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.553 |
LIG_HCF-1_HBM_1 | 377 | 380 | PF13415 | 0.451 |
LIG_LIR_Apic_2 | 308 | 312 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 344 | 355 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 390 | 401 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 409 | 417 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.426 |
LIG_NRBOX | 134 | 140 | PF00104 | 0.599 |
LIG_NRP_CendR_1 | 427 | 430 | PF00754 | 0.675 |
LIG_PCNA_yPIPBox_3 | 130 | 139 | PF02747 | 0.378 |
LIG_Pex14_1 | 407 | 411 | PF04695 | 0.411 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.500 |
LIG_SH2_CRK | 411 | 415 | PF00017 | 0.283 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.519 |
LIG_SH2_NCK_1 | 411 | 415 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 343 | 347 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 388 | 392 | PF00017 | 0.415 |
LIG_SH2_STAT3 | 165 | 168 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.406 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.385 |
LIG_SUMO_SIM_anti_2 | 240 | 246 | PF11976 | 0.530 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.441 |
LIG_TYR_ITIM | 345 | 350 | PF00017 | 0.501 |
LIG_Vh1_VBS_1 | 330 | 348 | PF01044 | 0.413 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.373 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.634 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.449 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.442 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.537 |
MOD_CMANNOS | 407 | 410 | PF00535 | 0.410 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.591 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.519 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.325 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.500 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.482 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.501 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.562 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.489 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.457 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.386 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.430 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.421 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.309 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.571 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.388 |
MOD_PKA_1 | 237 | 243 | PF00069 | 0.447 |
MOD_PKA_1 | 5 | 11 | PF00069 | 0.526 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.447 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.535 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.542 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.613 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.706 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.532 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.536 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.437 |
MOD_Plk_2-3 | 116 | 122 | PF00069 | 0.659 |
MOD_Plk_2-3 | 250 | 256 | PF00069 | 0.307 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.463 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.355 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.695 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.480 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.425 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.449 |
MOD_SUMO_for_1 | 170 | 173 | PF00179 | 0.562 |
MOD_SUMO_for_1 | 94 | 97 | PF00179 | 0.547 |
MOD_SUMO_rev_2 | 204 | 214 | PF00179 | 0.502 |
TRG_DiLeu_BaEn_1 | 51 | 56 | PF01217 | 0.518 |
TRG_DiLeu_BaEn_4 | 150 | 156 | PF01217 | 0.559 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.450 |
TRG_NES_CRM1_1 | 215 | 228 | PF08389 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 373 | 377 | PF00026 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0R4 | Leptomonas seymouri | 52% | 100% |
A0A0S4JD21 | Bodo saltans | 30% | 100% |
A0A1X0P4D8 | Trypanosomatidae | 37% | 100% |
A0A3Q8IGN6 | Leishmania donovani | 78% | 100% |
A0A422N3D5 | Trypanosoma rangeli | 37% | 100% |
A4I977 | Leishmania infantum | 78% | 100% |
D0A6D1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B418 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q406 | Leishmania major | 77% | 100% |
V5DQF0 | Trypanosoma cruzi | 36% | 100% |