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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B3V5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.485 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.349 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.342 |
DEG_SPOP_SBC_1 | 226 | 230 | PF00917 | 0.700 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.507 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.545 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.435 |
LIG_14-3-3_CanoR_1 | 23 | 27 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 267 | 271 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 276 | 285 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 321 | 327 | PF00244 | 0.495 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.458 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.336 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.624 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.487 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.401 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.332 |
LIG_HCF-1_HBM_1 | 75 | 78 | PF13415 | 0.447 |
LIG_Integrin_RGD_1 | 256 | 258 | PF01839 | 0.467 |
LIG_LIR_Gen_1 | 27 | 34 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.338 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.302 |
LIG_SH2_GRB2like | 184 | 187 | PF00017 | 0.320 |
LIG_SH2_SRC | 184 | 187 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.307 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.443 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.605 |
LIG_TYR_ITSM | 61 | 68 | PF00017 | 0.333 |
MOD_CDK_SPxxK_3 | 228 | 235 | PF00069 | 0.381 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.365 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.401 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.676 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.528 |
MOD_CMANNOS | 310 | 313 | PF00535 | 0.401 |
MOD_GlcNHglycan | 222 | 226 | PF01048 | 0.640 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.398 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.573 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.329 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.694 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.444 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.320 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.409 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.522 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.505 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.420 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.316 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.559 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.672 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.512 |
MOD_NEK2_2 | 322 | 327 | PF00069 | 0.501 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.469 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.302 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.350 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.493 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.333 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.387 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.359 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.521 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.457 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.306 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.492 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.314 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.326 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.404 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.437 |
MOD_SUMO_rev_2 | 228 | 237 | PF00179 | 0.606 |
TRG_DiLeu_BaEn_1 | 168 | 173 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.315 |
TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 307 | 312 | PF00026 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4F8 | Leptomonas seymouri | 81% | 95% |
A0A0S4J7D5 | Bodo saltans | 53% | 97% |
A0A1X0P104 | Trypanosomatidae | 63% | 100% |
A0A3Q8IGJ8 | Leishmania donovani | 97% | 100% |
A0A3R7N235 | Trypanosoma rangeli | 64% | 100% |
A4HLH6 | Leishmania braziliensis | 92% | 100% |
A4I8Y6 | Leishmania infantum | 96% | 100% |
D0A4Y3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
Q4Q469 | Leishmania major | 95% | 100% |
V5BZN0 | Trypanosoma cruzi | 63% | 100% |