Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QGQ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051170 | import into nucleus | 6 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 117 | 121 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.392 |
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.574 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.447 |
DEG_APCC_KENBOX_2 | 360 | 364 | PF00400 | 0.508 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.422 |
DEG_SPOP_SBC_1 | 340 | 344 | PF00917 | 0.605 |
DOC_CYCLIN_yCln2_LP_2 | 375 | 381 | PF00134 | 0.485 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.351 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.567 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 35 | 44 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 92 | 97 | PF00244 | 0.424 |
LIG_14-3-3_CterR_2 | 413 | 416 | PF00244 | 0.484 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 97 | 105 | PF00928 | 0.360 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.428 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.504 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.442 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.582 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.327 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.388 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.333 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.471 |
LIG_Integrin_RGD_1 | 62 | 64 | PF01839 | 0.496 |
LIG_LIR_Gen_1 | 146 | 152 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 169 | 176 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 249 | 260 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 304 | 315 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 95 | 106 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.351 |
LIG_PCNA_yPIPBox_3 | 24 | 37 | PF02747 | 0.491 |
LIG_PDZ_Class_2 | 411 | 416 | PF00595 | 0.468 |
LIG_Pex14_2 | 101 | 105 | PF04695 | 0.360 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.434 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.355 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.203 |
LIG_SH2_GRB2like | 44 | 47 | PF00017 | 0.281 |
LIG_SH2_NCK_1 | 183 | 187 | PF00017 | 0.410 |
LIG_SH2_SRC | 170 | 173 | PF00017 | 0.316 |
LIG_SH2_SRC | 398 | 401 | PF00017 | 0.316 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 20 | 23 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.459 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.390 |
LIG_SUMO_SIM_anti_2 | 217 | 222 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.337 |
MOD_CDC14_SPxK_1 | 190 | 193 | PF00782 | 0.457 |
MOD_CDK_SPxK_1 | 187 | 193 | PF00069 | 0.435 |
MOD_CDK_SPxxK_3 | 370 | 377 | PF00069 | 0.455 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.624 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.392 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.503 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.518 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.434 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.749 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.564 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.443 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.587 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.586 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.429 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.327 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.435 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.419 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.692 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.622 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.521 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.534 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.411 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.500 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.629 |
MOD_LATS_1 | 272 | 278 | PF00433 | 0.478 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.443 |
MOD_N-GLC_1 | 362 | 367 | PF02516 | 0.500 |
MOD_N-GLC_2 | 273 | 275 | PF02516 | 0.334 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.416 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.390 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.549 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.414 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.560 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.508 |
MOD_PKA_1 | 71 | 77 | PF00069 | 0.496 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.627 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.563 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.392 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.404 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.693 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.440 |
MOD_Plk_2-3 | 262 | 268 | PF00069 | 0.483 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.393 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.586 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.469 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.651 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.686 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.505 |
TRG_DiLeu_BaEn_4 | 99 | 105 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.478 |
TRG_NLS_MonoCore_2 | 68 | 73 | PF00514 | 0.513 |
TRG_NLS_MonoExtN_4 | 69 | 74 | PF00514 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6D9 | Leptomonas seymouri | 49% | 100% |
A0A1X0NR33 | Trypanosomatidae | 34% | 100% |
A0A3S7WRX1 | Leishmania donovani | 94% | 100% |
A0A422NA30 | Trypanosoma rangeli | 34% | 100% |
A4H6V4 | Leishmania braziliensis | 72% | 100% |
C9ZUI6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AGC6 | Leishmania infantum | 93% | 100% |
E9ANW6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5BTJ4 | Trypanosoma cruzi | 36% | 100% |