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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IUN5
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008483 | transaminase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016769 | transferase activity, transferring nitrogenous groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.587 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.512 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.332 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.509 |
DOC_CYCLIN_yCln2_LP_2 | 119 | 125 | PF00134 | 0.526 |
DOC_CYCLIN_yCln2_LP_2 | 362 | 368 | PF00134 | 0.449 |
DOC_MAPK_DCC_7 | 359 | 368 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 97 | 105 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 196 | 205 | PF00069 | 0.526 |
DOC_PP1_RVXF_1 | 156 | 163 | PF00149 | 0.482 |
DOC_PP1_RVXF_1 | 307 | 313 | PF00149 | 0.573 |
DOC_PP2B_LxvP_1 | 119 | 122 | PF13499 | 0.534 |
DOC_PP2B_LxvP_1 | 124 | 127 | PF13499 | 0.534 |
DOC_PP4_FxxP_1 | 176 | 179 | PF00568 | 0.512 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.482 |
DOC_USP7_MATH_2 | 127 | 133 | PF00917 | 0.467 |
DOC_USP7_UBL2_3 | 299 | 303 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.482 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 41 | 51 | PF00244 | 0.386 |
LIG_Actin_WH2_2 | 288 | 305 | PF00022 | 0.562 |
LIG_APCC_ABBA_1 | 326 | 331 | PF00400 | 0.420 |
LIG_BIR_III_2 | 84 | 88 | PF00653 | 0.635 |
LIG_EH1_1 | 36 | 44 | PF00400 | 0.257 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.530 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.496 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.575 |
LIG_LIR_Apic_2 | 174 | 179 | PF02991 | 0.559 |
LIG_LIR_Apic_2 | 245 | 250 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 86 | 96 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 282 | 287 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 57 | 61 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.474 |
LIG_PCNA_yPIPBox_3 | 155 | 163 | PF02747 | 0.593 |
LIG_Pex14_2 | 51 | 55 | PF04695 | 0.506 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.585 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.474 |
LIG_SH2_SRC | 141 | 144 | PF00017 | 0.544 |
LIG_SH2_SRC | 148 | 151 | PF00017 | 0.550 |
LIG_SH2_SRC | 338 | 341 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.525 |
LIG_SH2_STAT3 | 257 | 260 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.516 |
LIG_SUMO_SIM_anti_2 | 236 | 242 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 236 | 242 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 64 | 70 | PF11976 | 0.461 |
LIG_SxIP_EBH_1 | 155 | 169 | PF03271 | 0.526 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.513 |
LIG_UBA3_1 | 181 | 186 | PF00899 | 0.519 |
LIG_UBA3_1 | 274 | 281 | PF00899 | 0.575 |
LIG_WRC_WIRS_1 | 55 | 60 | PF05994 | 0.481 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.536 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.568 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.585 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.522 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.356 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.321 |
MOD_GlcNHglycan | 60 | 64 | PF01048 | 0.498 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.408 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.489 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.476 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.552 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.632 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.540 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.557 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.333 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.556 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.496 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.504 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.687 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.532 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.558 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.486 |
MOD_NEK2_2 | 190 | 195 | PF00069 | 0.542 |
MOD_NEK2_2 | 298 | 303 | PF00069 | 0.585 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.360 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.544 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.507 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.560 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.496 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.499 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.547 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.546 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.598 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.526 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.482 |
MOD_SUMO_for_1 | 358 | 361 | PF00179 | 0.320 |
MOD_SUMO_rev_2 | 304 | 311 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 356 | 360 | PF00179 | 0.513 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.526 |
TRG_DiLeu_BaEn_1 | 271 | 276 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_2 | 32 | 38 | PF01217 | 0.298 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDK5 | Leptomonas seymouri | 63% | 100% |
A0A1X0PAI4 | Trypanosomatidae | 38% | 100% |
A0A3R7NT31 | Trypanosoma rangeli | 36% | 100% |
A4HAV2 | Leishmania braziliensis | 82% | 100% |
A4I9Z9 | Leishmania infantum | 98% | 100% |
C9ZML4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 99% |
E9B527 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q2V9 | Leishmania major | 88% | 100% |
V5B0F3 | Trypanosoma cruzi | 33% | 82% |