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: 16 |
NetGPI | no | yes: 0, no: 16 |
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: E9AKX9
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008213 | protein alkylation | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016571 | histone methylation | 5 | 1 |
GO:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034968 | histone lysine methylation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010629 | negative regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0040029 | epigenetic regulation of gene expression | 6 | 1 |
GO:0045814 | negative regulation of gene expression, epigenetic | 7 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0008170 | N-methyltransferase activity | 5 | 2 |
GO:0008276 | protein methyltransferase activity | 3 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 2 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 2 |
GO:0042054 | histone methyltransferase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
GO:0042799 | histone H4K20 methyltransferase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.492 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.454 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.228 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.438 |
DEG_SPOP_SBC_1 | 105 | 109 | PF00917 | 0.513 |
DOC_MAPK_gen_1 | 449 | 459 | PF00069 | 0.428 |
DOC_PP2B_LxvP_1 | 339 | 342 | PF13499 | 0.450 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.492 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.569 |
LIG_14-3-3_CanoR_1 | 316 | 324 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 435 | 445 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 474 | 478 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 63 | 71 | PF00244 | 0.421 |
LIG_Actin_WH2_2 | 155 | 170 | PF00022 | 0.394 |
LIG_EH1_1 | 403 | 411 | PF00400 | 0.492 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.764 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.657 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.377 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.504 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.391 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.365 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.409 |
LIG_GBD_Chelix_1 | 365 | 373 | PF00786 | 0.228 |
LIG_LIR_Gen_1 | 385 | 395 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 385 | 390 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.424 |
LIG_SH2_CRK | 404 | 408 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 34 | 38 | PF00017 | 0.327 |
LIG_SH2_NCK_1 | 353 | 357 | PF00017 | 0.467 |
LIG_SH2_SRC | 353 | 356 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.332 |
LIG_SH2_STAT3 | 12 | 15 | PF00017 | 0.482 |
LIG_SH2_STAT3 | 20 | 23 | PF00017 | 0.356 |
LIG_SH2_STAT3 | 64 | 67 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.336 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.505 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.483 |
LIG_SUMO_SIM_par_1 | 123 | 132 | PF11976 | 0.511 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.384 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.433 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.654 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.359 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.482 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.376 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.332 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.401 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.543 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.403 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.288 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.391 |
MOD_DYRK1A_RPxSP_1 | 168 | 172 | PF00069 | 0.404 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.512 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.508 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.297 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.373 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.419 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.433 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.268 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.352 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.306 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.524 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.661 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.515 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.344 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.401 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.402 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.456 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.309 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.335 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.358 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.293 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.440 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.352 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.492 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.444 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.408 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.369 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.438 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.333 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.363 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.396 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.440 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.288 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.162 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.444 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.650 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.422 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.356 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.452 |
MOD_SUMO_for_1 | 133 | 136 | PF00179 | 0.482 |
MOD_SUMO_for_1 | 142 | 145 | PF00179 | 0.565 |
MOD_SUMO_rev_2 | 213 | 218 | PF00179 | 0.372 |
MOD_SUMO_rev_2 | 472 | 477 | PF00179 | 0.331 |
TRG_DiLeu_BaEn_1 | 204 | 209 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_4 | 472 | 478 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 203 | 208 | PF01217 | 0.288 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.323 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.262 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.313 |
TRG_NES_CRM1_1 | 382 | 394 | PF08389 | 0.259 |
TRG_Pf-PMV_PEXEL_1 | 449 | 453 | PF00026 | 0.321 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P571 | Leptomonas seymouri | 66% | 100% |
A0A0S4JRV8 | Bodo saltans | 39% | 100% |
A0A1X0NL17 | Trypanosomatidae | 47% | 100% |
A0A3R7KQ99 | Trypanosoma rangeli | 47% | 100% |
A0A3S7WPJ6 | Leishmania donovani | 91% | 99% |
A0A3S7WYH0 | Leishmania donovani | 25% | 100% |
A4H4R3 | Leishmania braziliensis | 80% | 100% |
A4HDM9 | Leishmania braziliensis | 28% | 100% |
A4HSZ2 | Leishmania infantum | 91% | 99% |
C9ZTM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AH76 | Leishmania infantum | 25% | 100% |
E9AX14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4QAG2 | Leishmania major | 27% | 100% |
Q4QIX6 | Leishmania major | 89% | 100% |
V5BT58 | Trypanosoma cruzi | 45% | 100% |