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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H6C5
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 3 |
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 | 3 |
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:0008168 | methyltransferase activity | 4 | 3 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008276 | protein methyltransferase activity | 3 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 1 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 1 |
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 | 1 |
GO:0042054 | histone methyltransferase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 384 | 388 | PF00656 | 0.591 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.779 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.767 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.746 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.716 |
CLV_PCSK_PC7_1 | 169 | 175 | PF00082 | 0.752 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.486 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.561 |
DEG_SCF_FBW7_1 | 273 | 280 | PF00400 | 0.515 |
DEG_SPOP_SBC_1 | 429 | 433 | PF00917 | 0.575 |
DEG_SPOP_SBC_1 | 436 | 440 | PF00917 | 0.544 |
DOC_CYCLIN_RxL_1 | 479 | 486 | PF00134 | 0.484 |
DOC_MAPK_gen_1 | 28 | 40 | PF00069 | 0.649 |
DOC_MAPK_gen_1 | 342 | 350 | PF00069 | 0.531 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.543 |
DOC_PP2B_PxIxI_1 | 50 | 56 | PF00149 | 0.494 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.489 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.434 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.758 |
LIG_14-3-3_CanoR_1 | 174 | 179 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 235 | 241 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 317 | 326 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 416 | 426 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 427 | 436 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 489 | 498 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.796 |
LIG_AP2alpha_2 | 323 | 325 | PF02296 | 0.400 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.755 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.521 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.712 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.401 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.548 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.585 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.514 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.591 |
LIG_LIR_Apic_2 | 123 | 127 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 464 | 473 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.446 |
LIG_Rb_pABgroove_1 | 377 | 385 | PF01858 | 0.557 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.556 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.510 |
LIG_SH2_CRK | 488 | 492 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.563 |
LIG_SH2_PTP2 | 467 | 470 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.427 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.625 |
LIG_SUMO_SIM_anti_2 | 52 | 58 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 378 | 385 | PF11976 | 0.561 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.616 |
LIG_TRAF2_1 | 459 | 462 | PF00917 | 0.490 |
LIG_TYR_ITIM | 465 | 470 | PF00017 | 0.568 |
LIG_WRC_WIRS_1 | 264 | 269 | PF05994 | 0.484 |
LIG_WRC_WIRS_1 | 470 | 475 | PF05994 | 0.375 |
LIG_WW_1 | 326 | 329 | PF00397 | 0.536 |
LIG_WW_3 | 325 | 329 | PF00397 | 0.590 |
MOD_CDC14_SPxK_1 | 119 | 122 | PF00782 | 0.395 |
MOD_CDK_SPxK_1 | 116 | 122 | PF00069 | 0.429 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.737 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.733 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.604 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.539 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.540 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.457 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.579 |
MOD_Cter_Amidation | 171 | 174 | PF01082 | 0.632 |
MOD_Cter_Amidation | 30 | 33 | PF01082 | 0.608 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.618 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.753 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.365 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.367 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.651 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.744 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.586 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.422 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.717 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.480 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.464 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.581 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.512 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.288 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.793 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.492 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.539 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.569 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.305 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.719 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.415 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.466 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.536 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.539 |
MOD_OFUCOSY | 190 | 196 | PF10250 | 0.259 |
MOD_OFUCOSY | 367 | 373 | PF10250 | 0.290 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.525 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.774 |
MOD_PK_1 | 174 | 180 | PF00069 | 0.684 |
MOD_PK_1 | 344 | 350 | PF00069 | 0.508 |
MOD_PKA_1 | 417 | 423 | PF00069 | 0.591 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.345 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.350 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.755 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.740 |
MOD_PKB_1 | 315 | 323 | PF00069 | 0.501 |
MOD_PKB_1 | 342 | 350 | PF00069 | 0.561 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.610 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.526 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.490 |
MOD_Plk_2-3 | 408 | 414 | PF00069 | 0.411 |
MOD_Plk_2-3 | 469 | 475 | PF00069 | 0.626 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.735 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.655 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.485 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.565 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.567 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.412 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.757 |
TRG_DiLeu_BaEn_2 | 485 | 491 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 184 | 189 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.410 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 498 | 501 | PF00400 | 0.571 |
TRG_NLS_MonoExtC_3 | 27 | 32 | PF00514 | 0.695 |
TRG_NLS_MonoExtN_4 | 25 | 32 | PF00514 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 482 | 486 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 67 | 72 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3I8 | Leptomonas seymouri | 49% | 91% |
A0A1X0NPE5 | Trypanosomatidae | 25% | 100% |
A0A3S5H671 | Leishmania donovani | 84% | 78% |
A0A3S5IRB9 | Trypanosoma rangeli | 29% | 100% |
A4HTM8 | Leishmania infantum | 84% | 99% |
C9ZPC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AMG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QI81 | Leishmania major | 86% | 100% |