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: A0A3S7WWY3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.603 |
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 6 | 10 | PF00656 | 0.366 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.423 |
DEG_APCC_DBOX_1 | 39 | 47 | PF00400 | 0.486 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.581 |
DEG_SPOP_SBC_1 | 154 | 158 | PF00917 | 0.555 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.636 |
DOC_CYCLIN_RxL_1 | 37 | 45 | PF00134 | 0.489 |
DOC_CYCLIN_yCln2_LP_2 | 22 | 28 | PF00134 | 0.458 |
DOC_PP1_RVXF_1 | 186 | 192 | PF00149 | 0.474 |
DOC_PP1_RVXF_1 | 225 | 231 | PF00149 | 0.423 |
DOC_PP2B_LxvP_1 | 81 | 84 | PF13499 | 0.510 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 153 | 163 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.371 |
LIG_BIR_III_4 | 166 | 170 | PF00653 | 0.587 |
LIG_CSL_BTD_1 | 81 | 84 | PF09270 | 0.517 |
LIG_CtBP_PxDLS_1 | 85 | 89 | PF00389 | 0.530 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.627 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.645 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.562 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.503 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.469 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.489 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.580 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.576 |
LIG_Integrin_isoDGR_2 | 31 | 33 | PF01839 | 0.437 |
LIG_LIR_Apic_2 | 103 | 109 | PF02991 | 0.610 |
LIG_LIR_Apic_2 | 45 | 50 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 265 | 273 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.417 |
LIG_NBox_RRM_1 | 7 | 17 | PF00076 | 0.377 |
LIG_NRBOX | 244 | 250 | PF00104 | 0.414 |
LIG_NRBOX | 7 | 13 | PF00104 | 0.487 |
LIG_RPA_C_Fungi | 166 | 178 | PF08784 | 0.554 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.544 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.635 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.512 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.553 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.438 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.670 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.636 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.587 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.515 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.634 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.419 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.466 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.599 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.686 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.515 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.597 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.628 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.557 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.601 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.487 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.546 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.608 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.621 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.459 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.692 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.388 |
MOD_PKB_1 | 151 | 159 | PF00069 | 0.647 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.727 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.470 |
MOD_Plk_2-3 | 3 | 9 | PF00069 | 0.477 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.648 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.559 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.589 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.669 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.549 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.763 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB35 | Leptomonas seymouri | 39% | 99% |
A4HC86 | Leishmania braziliensis | 62% | 100% |
A4HZR5 | Leishmania infantum | 99% | 100% |
E9AVM1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QBV8 | Leishmania major | 87% | 100% |