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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AIQ9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.678 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.472 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.662 |
CLV_PCSK_FUR_1 | 207 | 211 | PF00082 | 0.522 |
CLV_PCSK_FUR_1 | 312 | 316 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.664 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.464 |
CLV_PCSK_PC7_1 | 309 | 315 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.503 |
DEG_SCF_TRCP1_1 | 252 | 257 | PF00400 | 0.562 |
DEG_SPOP_SBC_1 | 296 | 300 | PF00917 | 0.642 |
DOC_CYCLIN_RxL_1 | 206 | 216 | PF00134 | 0.514 |
DOC_CYCLIN_RxL_1 | 217 | 227 | PF00134 | 0.409 |
DOC_MAPK_gen_1 | 146 | 152 | PF00069 | 0.500 |
DOC_PP1_RVXF_1 | 218 | 225 | PF00149 | 0.559 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.487 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.516 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.546 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 12 | 16 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 209 | 219 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 313 | 323 | PF00244 | 0.653 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.765 |
LIG_BRCT_BRCA1_1 | 252 | 256 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.499 |
LIG_CSL_BTD_1 | 190 | 193 | PF09270 | 0.514 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.668 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.549 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.488 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.661 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.620 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.530 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 286 | 290 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.606 |
LIG_LYPXL_yS_3 | 304 | 307 | PF13949 | 0.498 |
LIG_MLH1_MIPbox_1 | 3 | 7 | PF16413 | 0.499 |
LIG_PDZ_Class_2 | 325 | 330 | PF00595 | 0.499 |
LIG_Rb_LxCxE_1 | 172 | 194 | PF01857 | 0.587 |
LIG_SH2_SRC | 80 | 83 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.501 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.502 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.636 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.488 |
LIG_SUMO_SIM_par_1 | 229 | 237 | PF11976 | 0.481 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.507 |
LIG_TYR_ITIM | 302 | 307 | PF00017 | 0.493 |
MOD_CDC14_SPxK_1 | 15 | 18 | PF00782 | 0.659 |
MOD_CDC14_SPxK_1 | 29 | 32 | PF00782 | 0.502 |
MOD_CDK_SPxK_1 | 12 | 18 | PF00069 | 0.659 |
MOD_CDK_SPxK_1 | 26 | 32 | PF00069 | 0.503 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.694 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.661 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.689 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.664 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.653 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.661 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.687 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.661 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.581 |
MOD_GlcNHglycan | 107 | 111 | PF01048 | 0.779 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.721 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.807 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.534 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.582 |
MOD_GlcNHglycan | 58 | 62 | PF01048 | 0.579 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.652 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.600 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.620 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.769 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.679 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.627 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.500 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.439 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.436 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.591 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.625 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.506 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.723 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.636 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.658 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.625 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.644 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.614 |
MOD_NEK2_2 | 35 | 40 | PF00069 | 0.536 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.522 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.495 |
MOD_PKA_1 | 314 | 320 | PF00069 | 0.503 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.543 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.503 |
MOD_PKB_1 | 312 | 320 | PF00069 | 0.652 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.378 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.537 |
MOD_Plk_2-3 | 283 | 289 | PF00069 | 0.501 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.503 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.514 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.457 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.495 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.678 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.658 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.508 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.618 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.700 |
TRG_DiLeu_BaEn_4 | 19 | 25 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 207 | 212 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.656 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 311 | 314 | PF00400 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICW3 | Leishmania donovani | 65% | 86% |
A4I2B0 | Leishmania infantum | 65% | 87% |
E9AYF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 87% |
Q4Q915 | Leishmania major | 62% | 100% |