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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HNR6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.606 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.396 |
CLV_PCSK_FUR_1 | 157 | 161 | PF00082 | 0.609 |
CLV_PCSK_FUR_1 | 63 | 67 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.578 |
CLV_PCSK_PC7_1 | 99 | 105 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.494 |
DOC_MAPK_gen_1 | 238 | 246 | PF00069 | 0.462 |
DOC_MAPK_RevD_3 | 88 | 104 | PF00069 | 0.569 |
DOC_PP2B_LxvP_1 | 184 | 187 | PF13499 | 0.670 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.601 |
LIG_14-3-3_CanoR_1 | 127 | 133 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 139 | 145 | PF00244 | 0.445 |
LIG_APCC_ABBA_1 | 153 | 158 | PF00400 | 0.483 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.677 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.573 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.612 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.645 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.571 |
LIG_LIR_Gen_1 | 241 | 250 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.526 |
LIG_NRP_CendR_1 | 252 | 255 | PF00754 | 0.462 |
LIG_SH2_PTP2 | 243 | 246 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.674 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.697 |
LIG_SH2_STAT3 | 26 | 29 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.580 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.669 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.538 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.399 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.571 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.606 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.652 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.570 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.573 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.542 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.601 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.546 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.605 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.552 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.646 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.637 |
MOD_PIKK_1 | 77 | 83 | PF00454 | 0.548 |
MOD_PK_1 | 140 | 146 | PF00069 | 0.387 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.592 |
MOD_PKA_1 | 159 | 165 | PF00069 | 0.600 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.607 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.582 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.505 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.515 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.554 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.576 |
MOD_SUMO_for_1 | 216 | 219 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 122 | 128 | PF00179 | 0.612 |
TRG_DiLeu_BaEn_1 | 166 | 171 | PF01217 | 0.575 |
TRG_DiLeu_BaEn_4 | 23 | 29 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_4 | 241 | 247 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.496 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 116 | 121 | PF00026 | 0.607 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6Y9 | Leptomonas seymouri | 61% | 100% |
A0A1X0P948 | Trypanosomatidae | 30% | 100% |
A0A3R7P2R3 | Trypanosoma rangeli | 30% | 100% |
A0A3S7XAJ5 | Leishmania donovani | 81% | 83% |
A4ICS9 | Leishmania infantum | 81% | 83% |
D0A2M6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9ASH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q220 | Leishmania major | 81% | 100% |
V5DRQ0 | Trypanosoma cruzi | 29% | 100% |