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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HMI5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.409 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.563 |
DEG_APCC_DBOX_1 | 341 | 349 | PF00400 | 0.375 |
DEG_SCF_FBW7_1 | 114 | 121 | PF00400 | 0.566 |
DEG_SCF_FBW7_2 | 291 | 296 | PF00400 | 0.467 |
DEG_SPOP_SBC_1 | 120 | 124 | PF00917 | 0.557 |
DEG_SPOP_SBC_1 | 217 | 221 | PF00917 | 0.477 |
DOC_CKS1_1 | 33 | 38 | PF01111 | 0.526 |
DOC_PP4_FxxP_1 | 143 | 146 | PF00568 | 0.588 |
DOC_PP4_FxxP_1 | 157 | 160 | PF00568 | 0.548 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.523 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 149 | 154 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 84 | 89 | PF00244 | 0.585 |
LIG_Actin_WH2_2 | 292 | 308 | PF00022 | 0.678 |
LIG_APCC_ABBA_1 | 264 | 269 | PF00400 | 0.532 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.601 |
LIG_EH1_1 | 239 | 247 | PF00400 | 0.639 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.528 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.497 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.507 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.411 |
LIG_LIR_Apic_2 | 141 | 146 | PF02991 | 0.591 |
LIG_LIR_Apic_2 | 154 | 160 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 279 | 284 | PF02991 | 0.688 |
LIG_PDZ_Class_3 | 350 | 355 | PF00595 | 0.643 |
LIG_Pex14_2 | 264 | 268 | PF04695 | 0.671 |
LIG_SH2_SRC | 183 | 186 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.529 |
LIG_SH2_STAT3 | 238 | 241 | PF00017 | 0.425 |
LIG_SH2_STAT3 | 282 | 285 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.425 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.536 |
LIG_SUMO_SIM_anti_2 | 37 | 45 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 110 | 117 | PF11976 | 0.566 |
LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.493 |
LIG_WW_1 | 145 | 148 | PF00397 | 0.726 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.556 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.651 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.442 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.557 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.661 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.576 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.675 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.660 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.555 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.481 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.707 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.700 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.684 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.788 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.608 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.708 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.506 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.749 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.659 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.628 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.709 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.567 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.502 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.577 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.501 |
MOD_PK_1 | 149 | 155 | PF00069 | 0.551 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.724 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.590 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.474 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.624 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.493 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.633 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.551 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.595 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.718 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.468 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.526 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.724 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.669 |
TRG_DiLeu_BaLyEn_6 | 157 | 162 | PF01217 | 0.454 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.698 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.649 |
TRG_Pf-PMV_PEXEL_1 | 4 | 8 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKF7 | Leptomonas seymouri | 37% | 100% |
A0A3S7X929 | Leishmania donovani | 72% | 100% |
A4IB65 | Leishmania infantum | 72% | 100% |
E9AEY6 | Leishmania major | 72% | 100% |
E9B642 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 99% |