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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3Q8IDC8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.697 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.572 |
CLV_PCSK_FUR_1 | 176 | 180 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.563 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.461 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.559 |
DOC_CYCLIN_yCln2_LP_2 | 159 | 165 | PF00134 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 247 | 253 | PF00134 | 0.533 |
DOC_MAPK_gen_1 | 129 | 137 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 120 | 128 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 35 | 42 | PF00069 | 0.493 |
DOC_MAPK_NFAT4_5 | 35 | 43 | PF00069 | 0.490 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.549 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.712 |
LIG_14-3-3_CanoR_1 | 100 | 108 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 129 | 137 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 273 | 282 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 322 | 328 | PF00244 | 0.570 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.566 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.478 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.665 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.313 |
LIG_LIR_Apic_2 | 160 | 164 | PF02991 | 0.438 |
LIG_LIR_Apic_2 | 180 | 186 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 169 | 177 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.594 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.537 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.516 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.660 |
LIG_SH2_NCK_1 | 183 | 187 | PF00017 | 0.720 |
LIG_SH2_NCK_1 | 51 | 55 | PF00017 | 0.631 |
LIG_SH2_STAT3 | 10 | 13 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.549 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.645 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.470 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.547 |
LIG_SUMO_SIM_anti_2 | 217 | 223 | PF11976 | 0.502 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.576 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.481 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.468 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.520 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.640 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.567 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.590 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.741 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.664 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.654 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.588 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.489 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.422 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.628 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.694 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.486 |
MOD_NEK2_2 | 281 | 286 | PF00069 | 0.478 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.532 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.595 |
MOD_PKA_1 | 321 | 327 | PF00069 | 0.548 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.679 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.462 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.548 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.691 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.560 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.669 |
MOD_Plk_2-3 | 65 | 71 | PF00069 | 0.667 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.457 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.517 |
MOD_SUMO_rev_2 | 311 | 318 | PF00179 | 0.523 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.656 |
TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 135 | 138 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.446 |
TRG_NLS_MonoExtC_3 | 320 | 325 | PF00514 | 0.549 |
TRG_NLS_MonoExtN_4 | 321 | 326 | PF00514 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 278 | 283 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM80 | Leptomonas seymouri | 65% | 96% |
A0A1X0P627 | Trypanosomatidae | 37% | 100% |
A0A3R7NH36 | Trypanosoma rangeli | 44% | 100% |
A4HA69 | Leishmania braziliensis | 84% | 100% |
A4HYE1 | Leishmania infantum | 100% | 100% |
D0A0S6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AS74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QD92 | Leishmania major | 94% | 99% |
V5AZ17 | Trypanosoma cruzi | 43% | 100% |