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: 5 |
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: E9B1M6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 193 | 197 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.465 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.551 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.456 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.387 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.573 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.597 |
DOC_USP7_UBL2_3 | 130 | 134 | PF12436 | 0.577 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.526 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.451 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.464 |
LIG_Actin_WH2_2 | 93 | 110 | PF00022 | 0.531 |
LIG_APCC_ABBA_1 | 34 | 39 | PF00400 | 0.279 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.490 |
LIG_eIF4E_1 | 267 | 273 | PF01652 | 0.470 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.417 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.304 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.541 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.394 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.593 |
LIG_Integrin_RGD_1 | 194 | 196 | PF01839 | 0.473 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 264 | 275 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.535 |
LIG_NRBOX | 154 | 160 | PF00104 | 0.511 |
LIG_PCNA_yPIPBox_3 | 11 | 25 | PF02747 | 0.304 |
LIG_SH2_CRK | 267 | 271 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 267 | 271 | PF00017 | 0.535 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.584 |
LIG_SH2_STAT3 | 5 | 8 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.663 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.557 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.482 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.564 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.687 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.618 |
LIG_SUMO_SIM_par_1 | 179 | 186 | PF11976 | 0.404 |
LIG_TRFH_1 | 231 | 235 | PF08558 | 0.609 |
LIG_UBA3_1 | 169 | 177 | PF00899 | 0.479 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.507 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.503 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.702 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.643 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.476 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.489 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.482 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.455 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.552 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.732 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.633 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.486 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.616 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.607 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.415 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.441 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.353 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.506 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.641 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.552 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.664 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.516 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.418 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.506 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.557 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.482 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.490 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.478 |
MOD_SUMO_rev_2 | 140 | 148 | PF00179 | 0.512 |
MOD_SUMO_rev_2 | 286 | 295 | PF00179 | 0.649 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAJ7 | Leptomonas seymouri | 39% | 100% |
A0A0N1PCN3 | Leptomonas seymouri | 33% | 82% |
A0A3Q8IJW3 | Leishmania donovani | 83% | 100% |
A4HJ55 | Leishmania braziliensis | 65% | 100% |
A4I6G9 | Leishmania infantum | 84% | 100% |
Q9BHD3 | Leishmania major | 84% | 100% |