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: A4H4R3
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 | 268 | 272 | PF00656 | 0.492 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.442 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.304 |
CLV_Separin_Metazoa | 92 | 96 | PF03568 | 0.406 |
DEG_APCC_DBOX_1 | 150 | 158 | PF00400 | 0.342 |
DEG_APCC_DBOX_1 | 324 | 332 | PF00400 | 0.438 |
DEG_SPOP_SBC_1 | 106 | 110 | PF00917 | 0.490 |
DOC_CDC14_PxL_1 | 210 | 218 | PF14671 | 0.383 |
DOC_MAPK_gen_1 | 458 | 468 | PF00069 | 0.428 |
DOC_PP2B_LxvP_1 | 348 | 351 | PF13499 | 0.450 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.386 |
DOC_USP7_UBL2_3 | 477 | 481 | PF12436 | 0.288 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.577 |
LIG_14-3-3_CanoR_1 | 325 | 333 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 63 | 70 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.398 |
LIG_Actin_WH2_2 | 163 | 178 | PF00022 | 0.377 |
LIG_CaM_IQ_9 | 72 | 87 | PF13499 | 0.276 |
LIG_EH1_1 | 412 | 420 | PF00400 | 0.492 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.717 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.358 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.504 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.383 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.529 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.407 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.404 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.300 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.398 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.428 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.408 |
LIG_GBD_Chelix_1 | 374 | 382 | PF00786 | 0.228 |
LIG_LIR_Gen_1 | 114 | 123 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 394 | 404 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.458 |
LIG_PCNA_PIPBox_1 | 389 | 398 | PF02747 | 0.431 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 34 | 38 | PF00017 | 0.323 |
LIG_SH2_NCK_1 | 362 | 366 | PF00017 | 0.467 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 34 | 38 | PF00017 | 0.333 |
LIG_SH2_STAT3 | 12 | 15 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 20 | 23 | PF00017 | 0.347 |
LIG_SH2_STAT3 | 64 | 67 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.332 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.488 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.411 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.519 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.384 |
LIG_WW_3 | 203 | 207 | PF00397 | 0.280 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.636 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.660 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.246 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.268 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.387 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.399 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.482 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.422 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.451 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.401 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.401 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.542 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.403 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.288 |
MOD_DYRK1A_RPxSP_1 | 176 | 180 | PF00069 | 0.384 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.514 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.406 |
MOD_GlcNHglycan | 146 | 150 | PF01048 | 0.509 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.545 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.305 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.305 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.410 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.414 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.420 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.285 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.390 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.354 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.200 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.485 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.463 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.212 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.345 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.432 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.401 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.393 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.397 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.309 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.749 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.536 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.335 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.192 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.357 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.298 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.197 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.436 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.312 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.346 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.284 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.474 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.443 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.430 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.369 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.459 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.360 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.548 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.377 |
MOD_Plk_1 | 450 | 456 | PF00069 | 0.192 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.440 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.193 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.288 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.173 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.203 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.624 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.417 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.463 |
MOD_SUMO_rev_2 | 220 | 226 | PF00179 | 0.375 |
TRG_DiLeu_BaEn_1 | 212 | 217 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.288 |
TRG_DiLeu_BaLyEn_6 | 40 | 45 | PF01217 | 0.319 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.262 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P571 | Leptomonas seymouri | 62% | 100% |
A0A0S4JRV8 | Bodo saltans | 37% | 100% |
A0A1X0NL17 | Trypanosomatidae | 48% | 100% |
A0A3R7KQ99 | Trypanosoma rangeli | 46% | 100% |
A0A3S7WPJ6 | Leishmania donovani | 80% | 100% |
A0A3S7WYH0 | Leishmania donovani | 26% | 100% |
A4HDM9 | Leishmania braziliensis | 28% | 100% |
A4HSZ2 | Leishmania infantum | 80% | 100% |
C9ZTM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AH76 | Leishmania infantum | 26% | 100% |
E9AKX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9AX14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
Q4QAG2 | Leishmania major | 28% | 100% |
Q4QIX6 | Leishmania major | 79% | 100% |
V5BT58 | Trypanosoma cruzi | 44% | 100% |