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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ANW6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051170 | import into nucleus | 6 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 117 | 121 | PF00656 | 0.683 |
CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.423 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.616 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 350 | 352 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.469 |
DEG_SPOP_SBC_1 | 241 | 245 | PF00917 | 0.416 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.484 |
DOC_ANK_TNKS_1 | 350 | 357 | PF00023 | 0.463 |
DOC_CKS1_1 | 82 | 87 | PF01111 | 0.378 |
DOC_CYCLIN_yCln2_LP_2 | 359 | 365 | PF00134 | 0.543 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.371 |
DOC_USP7_UBL2_3 | 367 | 371 | PF12436 | 0.607 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 35 | 44 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 92 | 97 | PF00244 | 0.461 |
LIG_14-3-3_CterR_2 | 397 | 400 | PF00244 | 0.540 |
LIG_deltaCOP1_diTrp_1 | 97 | 105 | PF00928 | 0.381 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.224 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.445 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.499 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.524 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.362 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.408 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.356 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.490 |
LIG_LIR_Apic_2 | 182 | 186 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 146 | 152 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 169 | 176 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 304 | 315 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 95 | 106 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.372 |
LIG_PCNA_yPIPBox_3 | 24 | 37 | PF02747 | 0.501 |
LIG_PDZ_Class_2 | 395 | 400 | PF00595 | 0.526 |
LIG_Pex14_2 | 101 | 105 | PF04695 | 0.379 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.491 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.354 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.463 |
LIG_SH2_NCK_1 | 183 | 187 | PF00017 | 0.463 |
LIG_SH2_SRC | 170 | 173 | PF00017 | 0.337 |
LIG_SH2_SRC | 382 | 385 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.311 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.311 |
LIG_SH3_2 | 362 | 367 | PF14604 | 0.399 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.415 |
LIG_SUMO_SIM_anti_2 | 217 | 222 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.353 |
LIG_UBA3_1 | 252 | 258 | PF00899 | 0.267 |
MOD_CDC14_SPxK_1 | 190 | 193 | PF00782 | 0.503 |
MOD_CDK_SPxK_1 | 187 | 193 | PF00069 | 0.471 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.630 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.566 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.490 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.226 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.461 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.680 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.570 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.657 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.638 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.462 |
MOD_DYRK1A_RPxSP_1 | 339 | 343 | PF00069 | 0.452 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.602 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.615 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.523 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.346 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.498 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.322 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.410 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.468 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.500 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.512 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.433 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.484 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.600 |
MOD_LATS_1 | 272 | 278 | PF00433 | 0.532 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.360 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.413 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.410 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.546 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.432 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.280 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.564 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.565 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.636 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.586 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.650 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.433 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.433 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.498 |
MOD_Plk_2-3 | 262 | 268 | PF00069 | 0.506 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.418 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.402 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.551 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.579 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.533 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.645 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.521 |
TRG_DiLeu_BaEn_4 | 99 | 105 | PF01217 | 0.498 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.504 |
TRG_NES_CRM1_1 | 212 | 226 | PF08389 | 0.366 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6D9 | Leptomonas seymouri | 49% | 100% |
A0A1X0NR33 | Trypanosomatidae | 33% | 100% |
A0A3S7WRX1 | Leishmania donovani | 85% | 96% |
A0A422NA30 | Trypanosoma rangeli | 36% | 100% |
A4H6V4 | Leishmania braziliensis | 72% | 99% |
C9ZUI6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AGC6 | Leishmania infantum | 85% | 96% |
Q4QGQ4 | Leishmania major | 84% | 100% |
V5BTJ4 | Trypanosoma cruzi | 35% | 100% |