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: A4H774
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 266 | 270 | PF00656 | 0.713 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.698 |
CLV_PCSK_FUR_1 | 298 | 302 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.698 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.732 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.552 |
CLV_PCSK_PC7_1 | 56 | 62 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.724 |
DOC_CKS1_1 | 37 | 42 | PF01111 | 0.571 |
DOC_MAPK_MEF2A_6 | 25 | 32 | PF00069 | 0.455 |
DOC_PP4_FxxP_1 | 118 | 121 | PF00568 | 0.695 |
DOC_USP7_UBL2_3 | 111 | 115 | PF12436 | 0.592 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 304 | 310 | PF00244 | 0.407 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.671 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.645 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.583 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.501 |
LIG_LIR_Apic_2 | 160 | 166 | PF02991 | 0.679 |
LIG_LIR_Apic_2 | 35 | 40 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.510 |
LIG_REV1ctd_RIR_1 | 122 | 131 | PF16727 | 0.506 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.534 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.596 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.611 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.704 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.600 |
LIG_TRAF2_1 | 191 | 194 | PF00917 | 0.738 |
LIG_TRAF2_2 | 139 | 144 | PF00917 | 0.523 |
LIG_TYR_ITIM | 67 | 72 | PF00017 | 0.461 |
MOD_CDK_SPxxK_3 | 47 | 54 | PF00069 | 0.603 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.584 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.620 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.518 |
MOD_Cter_Amidation | 113 | 116 | PF01082 | 0.588 |
MOD_Cter_Amidation | 233 | 236 | PF01082 | 0.640 |
MOD_Cter_Amidation | 58 | 61 | PF01082 | 0.654 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.699 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.597 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.632 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.605 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.726 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.669 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.717 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.536 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.675 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.782 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.597 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.697 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.472 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.708 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.568 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.476 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.705 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.592 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.562 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.544 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.546 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.512 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.592 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.558 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.705 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.733 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.671 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.669 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.567 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.638 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.507 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.636 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.510 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.466 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I155 | Leptomonas seymouri | 45% | 100% |
A0A3Q8I8I3 | Leishmania donovani | 70% | 85% |
A4HVL4 | Leishmania infantum | 71% | 85% |
E9APB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 96% |
Q4QG68 | Leishmania major | 71% | 100% |