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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: A0A3Q8IE50
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.436 |
DEG_SPOP_SBC_1 | 59 | 63 | PF00917 | 0.417 |
DOC_PP1_RVXF_1 | 68 | 75 | PF00149 | 0.433 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.417 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.434 |
LIG_14-3-3_CanoR_1 | 100 | 105 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 52 | 60 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 70 | 75 | PF00244 | 0.435 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.436 |
LIG_EH1_1 | 6 | 14 | PF00400 | 0.348 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.410 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.369 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.391 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.347 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.433 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.399 |
LIG_LIR_Gen_1 | 61 | 72 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 80 | 90 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.435 |
LIG_NRBOX | 14 | 20 | PF00104 | 0.369 |
LIG_NRBOX | 93 | 99 | PF00104 | 0.388 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.429 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.436 |
LIG_SUMO_SIM_anti_2 | 11 | 17 | PF11976 | 0.358 |
LIG_SUMO_SIM_anti_2 | 91 | 98 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 11 | 17 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 86 | 93 | PF11976 | 0.400 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.397 |
LIG_TYR_ITIM | 81 | 86 | PF00017 | 0.433 |
LIG_Vh1_VBS_1 | 5 | 23 | PF01044 | 0.365 |
LIG_WW_3 | 26 | 30 | PF00397 | 0.451 |
MOD_CDC14_SPxK_1 | 26 | 29 | PF00782 | 0.446 |
MOD_CDC14_SPxK_1 | 37 | 40 | PF00782 | 0.476 |
MOD_CDK_SPxK_1 | 23 | 29 | PF00069 | 0.432 |
MOD_CDK_SPxK_1 | 34 | 40 | PF00069 | 0.482 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.441 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.402 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.464 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.365 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.477 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.466 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.463 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.400 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.371 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.461 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.416 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.434 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.435 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.387 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.369 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.478 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.387 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.466 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.432 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.482 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.431 |
TRG_NES_CRM1_1 | 11 | 24 | PF08389 | 0.376 |