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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4H7I9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.545 |
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.406 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.438 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.421 |
DEG_COP1_1 | 171 | 182 | PF00400 | 0.536 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.538 |
DOC_MAPK_gen_1 | 295 | 301 | PF00069 | 0.487 |
DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.475 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.589 |
DOC_USP7_UBL2_3 | 296 | 300 | PF12436 | 0.483 |
DOC_USP7_UBL2_3 | 85 | 89 | PF12436 | 0.458 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.648 |
LIG_14-3-3_CanoR_1 | 25 | 30 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 263 | 268 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 45 | 55 | PF00244 | 0.411 |
LIG_Actin_WH2_2 | 242 | 259 | PF00022 | 0.487 |
LIG_BIR_III_2 | 184 | 188 | PF00653 | 0.526 |
LIG_BRCT_BRCA1_1 | 270 | 274 | PF00533 | 0.285 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.439 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.233 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.531 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.395 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.375 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.468 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.475 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 277 | 284 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 28 | 35 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 277 | 281 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 28 | 32 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.373 |
LIG_NRBOX | 139 | 145 | PF00104 | 0.480 |
LIG_Pex14_1 | 104 | 108 | PF04695 | 0.301 |
LIG_Pex14_1 | 72 | 76 | PF04695 | 0.520 |
LIG_Pex14_2 | 274 | 278 | PF04695 | 0.416 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.313 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 47 | 50 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.389 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.761 |
LIG_SUMO_SIM_par_1 | 36 | 44 | PF11976 | 0.451 |
LIG_SxIP_EBH_1 | 9 | 23 | PF03271 | 0.479 |
LIG_TYR_ITIM | 118 | 123 | PF00017 | 0.468 |
MOD_CDK_SPK_2 | 145 | 150 | PF00069 | 0.566 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.458 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.689 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.667 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.286 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.536 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.465 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.448 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.683 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.363 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.424 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.259 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.737 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.694 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.549 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.390 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.506 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.465 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.683 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.438 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.507 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.460 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.489 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.402 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.587 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.377 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.465 |
MOD_PKA_1 | 263 | 269 | PF00069 | 0.435 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.465 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.435 |
MOD_PKB_1 | 25 | 33 | PF00069 | 0.464 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.417 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.508 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.476 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.433 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.468 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.578 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.641 |
MOD_SUMO_for_1 | 294 | 297 | PF00179 | 0.475 |
TRG_DiLeu_BaEn_1 | 289 | 294 | PF01217 | 0.457 |
TRG_DiLeu_BaEn_2 | 235 | 241 | PF01217 | 0.357 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.332 |
TRG_ER_diArg_1 | 24 | 27 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F1 | Leptomonas seymouri | 52% | 86% |
A0A3Q8IBX5 | Leishmania donovani | 85% | 100% |
A4HVX2 | Leishmania infantum | 85% | 100% |
C9ZT50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9APM3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QFV5 | Leishmania major | 85% | 100% |