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: 10 |
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 | yes | yes: 5, no: 1 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AQ54
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.689 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.424 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.515 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.524 |
DOC_CDC14_PxL_1 | 13 | 21 | PF14671 | 0.603 |
DOC_CKS1_1 | 178 | 183 | PF01111 | 0.395 |
DOC_CYCLIN_yCln2_LP_2 | 183 | 189 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 9 | 15 | PF00134 | 0.581 |
DOC_MAPK_gen_1 | 232 | 240 | PF00069 | 0.456 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.480 |
DOC_PP2B_LxvP_1 | 9 | 12 | PF13499 | 0.586 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.534 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.597 |
LIG_14-3-3_CanoR_1 | 316 | 321 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 44 | 52 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.367 |
LIG_APCC_ABBA_1 | 196 | 201 | PF00400 | 0.578 |
LIG_APCC_ABBAyCdc20_2 | 295 | 301 | PF00400 | 0.359 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.550 |
LIG_CSL_BTD_1 | 119 | 122 | PF09270 | 0.550 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.486 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.689 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.541 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.412 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.499 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.527 |
LIG_LIR_Gen_1 | 202 | 211 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.358 |
LIG_MYND_1 | 181 | 185 | PF01753 | 0.544 |
LIG_PCNA_yPIPBox_3 | 188 | 199 | PF02747 | 0.524 |
LIG_SH2_CRK | 205 | 209 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 106 | 110 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 205 | 209 | PF00017 | 0.517 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.474 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.550 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.495 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.545 |
LIG_SUMO_SIM_anti_2 | 22 | 27 | PF11976 | 0.609 |
LIG_SUMO_SIM_par_1 | 16 | 22 | PF11976 | 0.598 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.549 |
LIG_WRC_WIRS_1 | 92 | 97 | PF05994 | 0.421 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.427 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.529 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.535 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.401 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.560 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.553 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.507 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.559 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.756 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.690 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.633 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.699 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.609 |
MOD_GlcNHglycan | 48 | 52 | PF01048 | 0.752 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.716 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.562 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.516 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.538 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.555 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.476 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.461 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.370 |
MOD_N-GLC_2 | 260 | 262 | PF02516 | 0.605 |
MOD_N-GLC_2 | 69 | 71 | PF02516 | 0.593 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.595 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.359 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.562 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.520 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.604 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.496 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.494 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.585 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.416 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.462 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.463 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.532 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.406 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.522 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.569 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.596 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.681 |
TRG_DiLeu_BaLyEn_6 | 313 | 318 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P748 | Leptomonas seymouri | 38% | 100% |
A0A3S7WTK4 | Leishmania donovani | 81% | 100% |
A4H829 | Leishmania braziliensis | 63% | 100% |
A4HWF5 | Leishmania infantum | 81% | 100% |
Q4QFC8 | Leishmania major | 80% | 100% |