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: 1, no: 7 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3Q8II73
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 202 | 206 | PF00656 | 0.593 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.530 |
CLV_Separin_Metazoa | 15 | 19 | PF03568 | 0.524 |
DEG_SCF_FBW7_1 | 172 | 179 | PF00400 | 0.596 |
DEG_SPOP_SBC_1 | 176 | 180 | PF00917 | 0.536 |
DOC_CKS1_1 | 173 | 178 | PF01111 | 0.729 |
DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.478 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.626 |
DOC_PP4_MxPP_1 | 235 | 238 | PF00568 | 0.442 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.444 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 189 | 193 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.549 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.604 |
LIG_EVH1_1 | 146 | 150 | PF00568 | 0.434 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.473 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.525 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 90 | 96 | PF02991 | 0.624 |
LIG_LIR_Gen_1 | 115 | 124 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 31 | 39 | PF02991 | 0.482 |
LIG_LIR_LC3C_4 | 218 | 221 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 12 | 16 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.469 |
LIG_REV1ctd_RIR_1 | 41 | 49 | PF16727 | 0.410 |
LIG_SH2_PTP2 | 123 | 126 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.476 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.493 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.626 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.424 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.540 |
LIG_WRC_WIRS_1 | 113 | 118 | PF05994 | 0.311 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.367 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.656 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.506 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.563 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.502 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.512 |
MOD_Cter_Amidation | 226 | 229 | PF01082 | 0.448 |
MOD_DYRK1A_RPxSP_1 | 83 | 87 | PF00069 | 0.524 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.637 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.531 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.404 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.695 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.602 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.494 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.626 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.465 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.378 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.466 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.350 |
MOD_OFUCOSY | 128 | 135 | PF10250 | 0.416 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.398 |
MOD_PKA_1 | 228 | 234 | PF00069 | 0.360 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.427 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.516 |
MOD_PKB_1 | 52 | 60 | PF00069 | 0.484 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.450 |
MOD_Plk_2-3 | 256 | 262 | PF00069 | 0.409 |
MOD_Plk_2-3 | 9 | 15 | PF00069 | 0.515 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.359 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.458 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.662 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.395 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.709 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.587 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.540 |
MOD_SUMO_rev_2 | 208 | 216 | PF00179 | 0.478 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.500 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.463 |
TRG_NES_CRM1_1 | 66 | 81 | PF08389 | 0.464 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1X1 | Leptomonas seymouri | 38% | 97% |
A0A3R7KJU0 | Trypanosoma rangeli | 24% | 100% |
A4HN06 | Leishmania braziliensis | 74% | 100% |
A4IBM9 | Leishmania infantum | 98% | 100% |
E9AFG3 | Leishmania major | 90% | 100% |
E9B6L8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5BYA4 | Trypanosoma cruzi | 24% | 100% |