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:0005739 | mitochondrion | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9AVW6
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008170 | N-methyltransferase activity | 5 | 11 |
GO:0008276 | protein methyltransferase activity | 3 | 11 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 11 |
GO:0016273 | arginine N-methyltransferase activity | 6 | 11 |
GO:0016274 | protein-arginine N-methyltransferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0035243 | protein-arginine omega-N symmetric methyltransferase activity | 5 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004190 | aspartic-type endopeptidase activity | 5 | 1 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0070001 | aspartic-type peptidase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.339 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.502 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 56 | 58 | PF00082 | 0.570 |
CLV_PCSK_PC7_1 | 249 | 255 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.520 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.342 |
DEG_MDM2_SWIB_1 | 394 | 401 | PF02201 | 0.272 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.420 |
DOC_CYCLIN_yCln2_LP_2 | 303 | 309 | PF00134 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 425 | 431 | PF00134 | 0.339 |
DOC_MAPK_gen_1 | 253 | 261 | PF00069 | 0.274 |
DOC_MAPK_gen_1 | 416 | 425 | PF00069 | 0.291 |
DOC_MAPK_gen_1 | 60 | 70 | PF00069 | 0.500 |
DOC_MAPK_HePTP_8 | 251 | 263 | PF00069 | 0.315 |
DOC_MAPK_MEF2A_6 | 253 | 261 | PF00069 | 0.293 |
DOC_MAPK_RevD_3 | 413 | 427 | PF00069 | 0.328 |
DOC_PP1_RVXF_1 | 311 | 318 | PF00149 | 0.291 |
DOC_PP2B_LxvP_1 | 338 | 341 | PF13499 | 0.405 |
DOC_PP4_FxxP_1 | 148 | 151 | PF00568 | 0.429 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.445 |
DOC_USP7_UBL2_3 | 106 | 110 | PF12436 | 0.348 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.291 |
LIG_14-3-3_CanoR_1 | 112 | 122 | PF00244 | 0.423 |
LIG_CSL_BTD_1 | 371 | 374 | PF09270 | 0.272 |
LIG_deltaCOP1_diTrp_1 | 282 | 287 | PF00928 | 0.272 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.291 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.347 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.192 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.433 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.287 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.272 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.346 |
LIG_GBD_Chelix_1 | 259 | 267 | PF00786 | 0.405 |
LIG_LIR_Apic_2 | 116 | 122 | PF02991 | 0.429 |
LIG_LIR_Apic_2 | 145 | 151 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 320 | 329 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 397 | 406 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 495 | 503 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 90 | 97 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 397 | 401 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 495 | 500 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.346 |
LIG_LYPXL_yS_3 | 104 | 107 | PF13949 | 0.322 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.315 |
LIG_Pex14_2 | 394 | 398 | PF04695 | 0.272 |
LIG_Pex14_2 | 443 | 447 | PF04695 | 0.272 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.406 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.291 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.385 |
LIG_SH2_GRB2like | 314 | 317 | PF00017 | 0.405 |
LIG_SH2_SRC | 184 | 187 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 301 | 304 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.272 |
LIG_SH3_1 | 174 | 180 | PF00018 | 0.272 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.272 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.291 |
LIG_SUMO_SIM_anti_2 | 448 | 454 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 179 | 185 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 257 | 262 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 352 | 359 | PF11976 | 0.295 |
LIG_SUMO_SIM_par_1 | 47 | 55 | PF11976 | 0.524 |
LIG_TYR_ITIM | 452 | 457 | PF00017 | 0.328 |
LIG_UBA3_1 | 223 | 230 | PF00899 | 0.386 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.529 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.614 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.428 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.287 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.264 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.571 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.281 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.613 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.367 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.573 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.275 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.383 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.616 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.451 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.508 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.405 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.291 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.427 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.347 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.362 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.360 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.324 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.726 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.208 |
MOD_PK_1 | 342 | 348 | PF00069 | 0.251 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.251 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.367 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.328 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.272 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.390 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.315 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.421 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.291 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.351 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.561 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.352 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.378 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.291 |
TRG_DiLeu_BaLyEn_6 | 177 | 182 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 489 | 494 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.478 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.379 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.256 |
TRG_NLS_MonoExtN_4 | 106 | 113 | PF00514 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3E5 | Leptomonas seymouri | 85% | 83% |
A0A0S4JG91 | Bodo saltans | 60% | 99% |
A0A1X0NTX7 | Trypanosomatidae | 67% | 85% |
A0A3S7WXD7 | Leishmania donovani | 97% | 100% |
A4HCH2 | Leishmania braziliensis | 92% | 100% |
C9ZSP5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 86% |
E9AH02 | Leishmania infantum | 97% | 100% |
Q4QBL3 | Leishmania major | 97% | 100% |
V5D4I8 | Trypanosoma cruzi | 71% | 85% |