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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AJF8
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0032446 | protein modification by small protein conjugation | 6 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0045116 | protein neddylation | 7 | 11 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 11 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0019781 | NEDD8 activating enzyme activity | 3 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016746 | acyltransferase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 179 | 185 | PF00089 | 0.272 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.469 |
CLV_PCSK_FUR_1 | 267 | 271 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.469 |
CLV_PCSK_PC7_1 | 264 | 270 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.303 |
DEG_SPOP_SBC_1 | 164 | 168 | PF00917 | 0.156 |
DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.370 |
DOC_MAPK_DCC_7 | 334 | 342 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 442 | 450 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.287 |
DOC_MAPK_MEF2A_6 | 334 | 342 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 38 | 47 | PF00069 | 0.253 |
DOC_MAPK_MEF2A_6 | 442 | 450 | PF00069 | 0.507 |
DOC_PP2B_LxvP_1 | 430 | 433 | PF13499 | 0.448 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.422 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.366 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.322 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 443 | 449 | PF00244 | 0.222 |
LIG_14-3-3_CanoR_1 | 469 | 476 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 511 | 518 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 8 | 18 | PF00244 | 0.544 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.589 |
LIG_BRCT_BRCA1_1 | 24 | 28 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.299 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.257 |
LIG_Clathr_ClatBox_1 | 136 | 140 | PF01394 | 0.414 |
LIG_deltaCOP1_diTrp_1 | 39 | 42 | PF00928 | 0.414 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.386 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.378 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.301 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.374 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.361 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.279 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.447 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.303 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.303 |
LIG_LIR_Gen_1 | 131 | 139 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 64 | 74 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 75 | 82 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.303 |
LIG_NRBOX | 56 | 62 | PF00104 | 0.414 |
LIG_PCNA_yPIPBox_3 | 509 | 519 | PF02747 | 0.352 |
LIG_PDZ_Class_2 | 520 | 525 | PF00595 | 0.565 |
LIG_Pex14_2 | 128 | 132 | PF04695 | 0.303 |
LIG_Pex14_2 | 488 | 492 | PF04695 | 0.532 |
LIG_PTB_Apo_2 | 365 | 372 | PF02174 | 0.376 |
LIG_SH2_GRB2like | 381 | 384 | PF00017 | 0.317 |
LIG_SH2_NCK_1 | 381 | 385 | PF00017 | 0.350 |
LIG_SH2_PTP2 | 253 | 256 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.337 |
LIG_SH3_1 | 291 | 297 | PF00018 | 0.272 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.421 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.300 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.350 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.419 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.548 |
LIG_SUMO_SIM_par_1 | 135 | 141 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 409 | 414 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 59 | 64 | PF11976 | 0.314 |
LIG_TYR_ITIM | 251 | 256 | PF00017 | 0.447 |
LIG_WRC_WIRS_1 | 129 | 134 | PF05994 | 0.370 |
MOD_CDC14_SPxK_1 | 5 | 8 | PF00782 | 0.415 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.635 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.669 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.495 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.464 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.220 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.279 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.447 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.434 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.572 |
MOD_GlcNHglycan | 414 | 418 | PF01048 | 0.204 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.565 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.577 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.484 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.303 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.414 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.245 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.303 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.414 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.671 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.421 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.670 |
MOD_PKA_1 | 268 | 274 | PF00069 | 0.447 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.303 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.449 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.496 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.331 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.529 |
MOD_Plk_2-3 | 286 | 292 | PF00069 | 0.156 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.371 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.487 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.414 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.366 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.640 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.391 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.322 |
MOD_SUMO_rev_2 | 185 | 194 | PF00179 | 0.428 |
TRG_DiLeu_BaEn_1 | 189 | 194 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_1 | 56 | 61 | PF01217 | 0.379 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 441 | 443 | PF00400 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 401 | 406 | PF00026 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIU8 | Leptomonas seymouri | 64% | 99% |
A0A1X0P2L8 | Trypanosomatidae | 40% | 100% |
A0A3S7WNL1 | Leishmania donovani | 91% | 97% |
A0A422NGT4 | Trypanosoma rangeli | 45% | 100% |
A4H389 | Leishmania braziliensis | 81% | 100% |
A4HRJ4 | Leishmania infantum | 91% | 97% |
C9ZXM5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AC62 | Leishmania major | 88% | 100% |
O65041 | Arabidopsis thaliana | 34% | 100% |
Q09765 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q5R4A0 | Pongo abelii | 36% | 100% |
Q7ZVX6 | Danio rerio | 36% | 100% |
Q8C878 | Mus musculus | 36% | 100% |
Q8TBC4 | Homo sapiens | 36% | 100% |
Q99MI7 | Rattus norvegicus | 36% | 100% |
Q9V6U8 | Drosophila melanogaster | 33% | 100% |
V5BH30 | Trypanosoma cruzi | 48% | 100% |