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: 5 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 4, no: 6 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H9G3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.508 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.407 |
DEG_SCF_FBW7_1 | 155 | 161 | PF00400 | 0.575 |
DOC_CKS1_1 | 155 | 160 | PF01111 | 0.519 |
DOC_MAPK_gen_1 | 298 | 310 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 332 | 341 | PF00069 | 0.593 |
DOC_PP1_RVXF_1 | 341 | 348 | PF00149 | 0.558 |
DOC_PP1_RVXF_1 | 85 | 92 | PF00149 | 0.489 |
DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.403 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.715 |
DOC_USP7_UBL2_3 | 300 | 304 | PF12436 | 0.646 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 122 | 127 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 192 | 202 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 240 | 247 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 306 | 311 | PF00244 | 0.566 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.496 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.518 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.489 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.466 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.579 |
LIG_LIR_Gen_1 | 20 | 30 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 344 | 350 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.500 |
LIG_PDZ_Class_1 | 345 | 350 | PF00595 | 0.609 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.517 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.421 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.521 |
LIG_SH2_GRB2like | 59 | 62 | PF00017 | 0.545 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.478 |
LIG_SH2_NCK_1 | 23 | 27 | PF00017 | 0.380 |
LIG_SH2_PTP2 | 73 | 76 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.290 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.507 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.750 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.572 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.290 |
LIG_TYR_ITIM | 21 | 26 | PF00017 | 0.494 |
LIG_UBA3_1 | 229 | 237 | PF00899 | 0.379 |
LIG_WRC_WIRS_1 | 127 | 132 | PF05994 | 0.539 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.433 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.426 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.341 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.529 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.649 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.336 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.569 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.595 |
MOD_Cter_Amidation | 120 | 123 | PF01082 | 0.468 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.456 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.406 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.457 |
MOD_GlcNHglycan | 252 | 256 | PF01048 | 0.642 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.429 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.356 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.485 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.392 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.484 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.464 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.515 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.510 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.432 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.506 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.520 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.537 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.478 |
MOD_NEK2_2 | 146 | 151 | PF00069 | 0.387 |
MOD_PK_1 | 122 | 128 | PF00069 | 0.532 |
MOD_PK_1 | 37 | 43 | PF00069 | 0.348 |
MOD_PKA_1 | 122 | 128 | PF00069 | 0.407 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.667 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.566 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.532 |
MOD_Plk_2-3 | 337 | 343 | PF00069 | 0.386 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.471 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.464 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.526 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.496 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.630 |
MOD_SUMO_for_1 | 67 | 70 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 223 | 230 | PF00179 | 0.633 |
MOD_SUMO_rev_2 | 82 | 89 | PF00179 | 0.530 |
TRG_DiLeu_BaEn_1 | 112 | 117 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_1 | 226 | 231 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.522 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 266 | 270 | PF00026 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDN8 | Leptomonas seymouri | 47% | 80% |
A0A0S4J078 | Bodo saltans | 23% | 75% |
A0A1X0P6U2 | Trypanosomatidae | 27% | 79% |
A0A3S7WUV0 | Leishmania donovani | 73% | 99% |
A0A422NJ54 | Trypanosoma rangeli | 28% | 78% |
A4HXT0 | Leishmania infantum | 73% | 99% |
D0A062 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 78% |
E9ARJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 98% |
Q4QDY7 | Leishmania major | 71% | 100% |