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: A4HZE9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.435 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.460 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.509 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.533 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.690 |
DOC_USP7_UBL2_3 | 234 | 238 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 249 | 258 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 51 | 60 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 81 | 91 | PF00244 | 0.408 |
LIG_BIR_III_2 | 187 | 191 | PF00653 | 0.662 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.542 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.466 |
LIG_LIR_Gen_1 | 139 | 146 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.430 |
LIG_SH2_NCK_1 | 259 | 263 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.459 |
LIG_SH3_1 | 77 | 83 | PF00018 | 0.446 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.681 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.426 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.519 |
MOD_CDK_SPxxK_3 | 141 | 148 | PF00069 | 0.468 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.528 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.515 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.614 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.391 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.499 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.631 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.625 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.548 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.472 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.427 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.563 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.458 |
MOD_Cter_Amidation | 234 | 237 | PF01082 | 0.567 |
MOD_Cter_Amidation | 25 | 28 | PF01082 | 0.584 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.592 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.754 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.446 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.724 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.568 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.652 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.398 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.552 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.538 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.528 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.634 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.556 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.549 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.724 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.483 |
MOD_NEK2_2 | 46 | 51 | PF00069 | 0.602 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.567 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.590 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.584 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.650 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.520 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.541 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.717 |
MOD_SUMO_rev_2 | 252 | 258 | PF00179 | 0.520 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.429 |
TRG_NLS_MonoExtC_3 | 75 | 80 | PF00514 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.594 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAX4 | Leptomonas seymouri | 32% | 94% |
A0A3Q8IL79 | Leishmania donovani | 99% | 100% |
A4HC00 | Leishmania braziliensis | 60% | 99% |
E9AVD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QC43 | Leishmania major | 88% | 100% |