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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4Q254
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.391 |
CLV_C14_Caspase3-7 | 25 | 29 | PF00656 | 0.459 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.392 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.420 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.664 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.509 |
DOC_CYCLIN_RxL_1 | 183 | 196 | PF00134 | 0.416 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.521 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 174 | 178 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 58 | 67 | PF00244 | 0.615 |
LIG_Actin_WH2_2 | 152 | 169 | PF00022 | 0.434 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.436 |
LIG_eIF4E_1 | 104 | 110 | PF01652 | 0.482 |
LIG_eIF4E_1 | 87 | 93 | PF01652 | 0.501 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.570 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.494 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.625 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.442 |
LIG_MYND_1 | 94 | 98 | PF01753 | 0.423 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.415 |
LIG_SH3_2 | 67 | 72 | PF14604 | 0.597 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.672 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.667 |
LIG_SUMO_SIM_anti_2 | 105 | 112 | PF11976 | 0.392 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.444 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.493 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.548 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.651 |
MOD_DYRK1A_RPxSP_1 | 63 | 67 | PF00069 | 0.726 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.520 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.580 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.559 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.708 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.446 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.448 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.399 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.503 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.453 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.650 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.624 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.446 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.644 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.519 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.657 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.424 |
MOD_SUMO_for_1 | 155 | 158 | PF00179 | 0.448 |
TRG_DiLeu_BaEn_1 | 88 | 93 | PF01217 | 0.494 |
TRG_ER_diArg_1 | 51 | 54 | PF00400 | 0.603 |
TRG_NES_CRM1_1 | 140 | 154 | PF08389 | 0.307 |
TRG_Pf-PMV_PEXEL_1 | 139 | 143 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5U6 | Leptomonas seymouri | 62% | 98% |
A0A1X0P8P1 | Trypanosomatidae | 38% | 97% |
A0A3Q8IQF0 | Leishmania donovani | 96% | 100% |
A0A422P2B9 | Trypanosoma rangeli | 41% | 98% |
A4HNN2 | Leishmania braziliensis | 80% | 100% |
A4ICW3 | Leishmania infantum | 96% | 100% |
E9ASE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |