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: Q4QIX6
Term | Name | Level | Count |
---|---|---|---|
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010629 | negative regulation of gene expression | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0040029 | epigenetic regulation of gene expression | 6 | 2 |
GO:0045814 | negative regulation of gene expression, epigenetic | 7 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0005488 | binding | 1 | 10 |
GO:0008168 | methyltransferase activity | 4 | 3 |
GO:0008170 | N-methyltransferase activity | 5 | 3 |
GO:0008276 | protein methyltransferase activity | 3 | 3 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 3 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 3 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 3 |
GO:0042054 | histone methyltransferase activity | 4 | 3 |
GO:0042799 | histone H4K20 methyltransferase activity | 6 | 2 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 266 | 270 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.238 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.487 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.330 |
DEG_APCC_DBOX_1 | 322 | 330 | PF00400 | 0.461 |
DEG_SPOP_SBC_1 | 105 | 109 | PF00917 | 0.523 |
DOC_MAPK_gen_1 | 456 | 466 | PF00069 | 0.451 |
DOC_PP2B_LxvP_1 | 346 | 349 | PF13499 | 0.475 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.518 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 323 | 331 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 442 | 452 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 63 | 71 | PF00244 | 0.454 |
LIG_Actin_WH2_2 | 162 | 177 | PF00022 | 0.434 |
LIG_EH1_1 | 410 | 418 | PF00400 | 0.518 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.496 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.723 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.403 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.529 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.417 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.403 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.365 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.371 |
LIG_GBD_Chelix_1 | 372 | 380 | PF00786 | 0.251 |
LIG_LIR_Gen_1 | 392 | 402 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 462 | 468 | PF02991 | 0.446 |
LIG_NRBOX | 392 | 398 | PF00104 | 0.537 |
LIG_PCNA_PIPBox_1 | 387 | 396 | PF02747 | 0.454 |
LIG_PCNA_TLS_4 | 445 | 452 | PF02747 | 0.397 |
LIG_SH2_CRK | 411 | 415 | PF00017 | 0.469 |
LIG_SH2_NCK_1 | 34 | 38 | PF00017 | 0.367 |
LIG_SH2_NCK_1 | 360 | 364 | PF00017 | 0.493 |
LIG_SH2_SRC | 360 | 363 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.342 |
LIG_SH2_STAT3 | 12 | 15 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 20 | 23 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.482 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.508 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.425 |
LIG_TYR_ITIM | 409 | 414 | PF00017 | 0.210 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.766 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.401 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.492 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.409 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.311 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.430 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.431 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.487 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.420 |
MOD_DYRK1A_RPxSP_1 | 101 | 105 | PF00069 | 0.432 |
MOD_DYRK1A_RPxSP_1 | 175 | 179 | PF00069 | 0.441 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.423 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.530 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.333 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.277 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.413 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.430 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.290 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.353 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.327 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.727 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.568 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.545 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.505 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.378 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.384 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.478 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.345 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.346 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.252 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.382 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.467 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.390 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.522 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.475 |
MOD_PK_1 | 235 | 241 | PF00069 | 0.269 |
MOD_PKA_1 | 234 | 240 | PF00069 | 0.469 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.540 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.537 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.447 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.375 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.269 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.459 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.431 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.392 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.461 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.323 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.162 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.543 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.703 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.435 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.391 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.497 |
MOD_SUMO_for_1 | 133 | 136 | PF00179 | 0.430 |
MOD_SUMO_for_1 | 149 | 152 | PF00179 | 0.596 |
MOD_SUMO_rev_2 | 477 | 484 | PF00179 | 0.357 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.430 |
TRG_DiLeu_BaEn_4 | 479 | 485 | PF01217 | 0.353 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.360 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.283 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.210 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.374 |
TRG_NES_CRM1_1 | 389 | 401 | PF08389 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 456 | 460 | PF00026 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P571 | Leptomonas seymouri | 65% | 100% |
A0A0S4JRV8 | Bodo saltans | 39% | 100% |
A0A1X0NL17 | Trypanosomatidae | 48% | 100% |
A0A3R7KQ99 | Trypanosoma rangeli | 46% | 100% |
A0A3S7WPJ6 | Leishmania donovani | 94% | 100% |
A0A3S7WYH0 | Leishmania donovani | 26% | 100% |
A4H4R3 | Leishmania braziliensis | 79% | 100% |
A4HDM9 | Leishmania braziliensis | 28% | 100% |
A4HSZ2 | Leishmania infantum | 95% | 100% |
C9ZTM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AH76 | Leishmania infantum | 26% | 100% |
E9AKX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AX14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4QAG2 | Leishmania major | 28% | 100% |
V5BT58 | Trypanosoma cruzi | 45% | 100% |