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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HBN7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.307 |
CLV_PCSK_FUR_1 | 175 | 179 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.368 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.447 |
DEG_SCF_FBW7_1 | 262 | 267 | PF00400 | 0.498 |
DEG_SCF_FBW7_2 | 281 | 288 | PF00400 | 0.441 |
DEG_SPOP_SBC_1 | 117 | 121 | PF00917 | 0.517 |
DOC_CKS1_1 | 202 | 207 | PF01111 | 0.324 |
DOC_CKS1_1 | 282 | 287 | PF01111 | 0.442 |
DOC_MAPK_gen_1 | 175 | 184 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 217 | 227 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 220 | 227 | PF00069 | 0.324 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.438 |
DOC_PP4_FxxP_1 | 202 | 205 | PF00568 | 0.346 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.332 |
DOC_USP7_UBL2_3 | 85 | 89 | PF12436 | 0.507 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 220 | 224 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 248 | 258 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 300 | 309 | PF00244 | 0.393 |
LIG_Actin_RPEL_3 | 213 | 232 | PF02755 | 0.405 |
LIG_APCC_ABBA_1 | 225 | 230 | PF00400 | 0.347 |
LIG_APCC_Cbox_2 | 39 | 45 | PF00515 | 0.451 |
LIG_BIR_III_4 | 111 | 115 | PF00653 | 0.580 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.391 |
LIG_EH1_1 | 220 | 228 | PF00400 | 0.386 |
LIG_EVH1_2 | 90 | 94 | PF00568 | 0.463 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.517 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.428 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.478 |
LIG_G3BP_FGDF_1 | 197 | 202 | PF02136 | 0.481 |
LIG_LIR_Apic_2 | 201 | 205 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 341 | 352 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.447 |
LIG_PDZ_Class_3 | 352 | 357 | PF00595 | 0.387 |
LIG_Pex14_2 | 17 | 21 | PF04695 | 0.371 |
LIG_Pex14_2 | 238 | 242 | PF04695 | 0.454 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.379 |
LIG_SH2_CRK | 309 | 313 | PF00017 | 0.353 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.324 |
LIG_SH2_STAT3 | 221 | 224 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.435 |
LIG_SH3_2 | 265 | 270 | PF14604 | 0.616 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.513 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.622 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.493 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.303 |
LIG_SUMO_SIM_par_1 | 48 | 54 | PF11976 | 0.433 |
LIG_TYR_ITIM | 226 | 231 | PF00017 | 0.316 |
LIG_UBA3_1 | 1 | 5 | PF00899 | 0.375 |
LIG_WRC_WIRS_1 | 199 | 204 | PF05994 | 0.460 |
LIG_WRC_WIRS_1 | 295 | 300 | PF05994 | 0.468 |
MOD_CDC14_SPxK_1 | 267 | 270 | PF00782 | 0.490 |
MOD_CDK_SPxK_1 | 264 | 270 | PF00069 | 0.495 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.506 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.326 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.473 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.517 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.535 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.343 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.465 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.374 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.404 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.523 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.469 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.483 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.557 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.536 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.302 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.570 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.453 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.462 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.464 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.514 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.443 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.255 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.462 |
MOD_PKB_1 | 6 | 14 | PF00069 | 0.436 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.446 |
MOD_Plk_2-3 | 286 | 292 | PF00069 | 0.498 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.473 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.390 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.392 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.488 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.341 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.554 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.614 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.634 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.494 |
MOD_SUMO_rev_2 | 319 | 329 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 39 | 49 | PF00179 | 0.435 |
MOD_SUMO_rev_2 | 80 | 87 | PF00179 | 0.548 |
TRG_DiLeu_BaEn_4 | 131 | 137 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.311 |
TRG_NES_CRM1_1 | 132 | 144 | PF08389 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 181 | 186 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2D3 | Leptomonas seymouri | 64% | 92% |
A0A1X0NXF1 | Trypanosomatidae | 42% | 100% |
A0A3Q8IDU8 | Leishmania donovani | 88% | 100% |
A4HZ38 | Leishmania infantum | 88% | 100% |
D0A1N9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AV06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QCH6 | Leishmania major | 88% | 100% |