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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 4 |
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: E9AZ41
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 113 | 117 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.525 |
CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.544 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.658 |
CLV_PCSK_FUR_1 | 266 | 270 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.623 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.644 |
DEG_SPOP_SBC_1 | 230 | 234 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.516 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.494 |
LIG_14-3-3_CanoR_1 | 166 | 171 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 217 | 227 | PF00244 | 0.753 |
LIG_14-3-3_CterR_2 | 266 | 271 | PF00244 | 0.516 |
LIG_Actin_RPEL_3 | 31 | 50 | PF02755 | 0.376 |
LIG_Actin_WH2_2 | 56 | 73 | PF00022 | 0.550 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.508 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.560 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.528 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.462 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.623 |
LIG_IBAR_NPY_1 | 180 | 182 | PF08397 | 0.657 |
LIG_LIR_Gen_1 | 116 | 127 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.689 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.691 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.505 |
LIG_SH2_STAT3 | 144 | 147 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.438 |
LIG_SH3_2 | 9 | 14 | PF14604 | 0.566 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.679 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.567 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.583 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.600 |
LIG_SxIP_EBH_1 | 241 | 252 | PF03271 | 0.524 |
LIG_UBA3_1 | 49 | 53 | PF00899 | 0.378 |
LIG_WW_3 | 10 | 14 | PF00397 | 0.564 |
MOD_CDC14_SPxK_1 | 214 | 217 | PF00782 | 0.639 |
MOD_CDK_SPxK_1 | 211 | 217 | PF00069 | 0.638 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.650 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.721 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.651 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.667 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.521 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.608 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.617 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.553 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.656 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.666 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.726 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.468 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.542 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.441 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.682 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.529 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.527 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.521 |
MOD_NEK2_2 | 66 | 71 | PF00069 | 0.477 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.527 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.522 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.527 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.551 |
MOD_PK_1 | 166 | 172 | PF00069 | 0.620 |
MOD_PKA_1 | 166 | 172 | PF00069 | 0.620 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.767 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.450 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.443 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.473 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.606 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.650 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.650 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.495 |
MOD_SUMO_rev_2 | 54 | 62 | PF00179 | 0.478 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 266 | 269 | PF00400 | 0.748 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIX8 | Leptomonas seymouri | 39% | 75% |
A0A3Q8IEA3 | Leishmania donovani | 82% | 86% |
A4HFR2 | Leishmania braziliensis | 55% | 100% |
A4I2T8 | Leishmania infantum | 82% | 86% |
E9ADB6 | Leishmania major | 79% | 100% |