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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q7U0
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008213 | protein alkylation | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0018022 | peptidyl-lysine methylation | 5 | 2 |
GO:0018026 | peptidyl-lysine monomethylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018205 | peptidyl-lysine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032259 | methylation | 2 | 11 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043414 | macromolecule methylation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
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 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 469 | 473 | PF00656 | 0.725 |
CLV_C14_Caspase3-7 | 87 | 91 | PF00656 | 0.483 |
CLV_MEL_PAP_1 | 608 | 614 | PF00089 | 0.362 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.381 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 309 | 311 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 33 | 35 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 615 | 617 | PF00082 | 0.319 |
CLV_PCSK_PC7_1 | 268 | 274 | PF00082 | 0.463 |
CLV_PCSK_PC7_1 | 611 | 617 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.392 |
DEG_APCC_DBOX_1 | 208 | 216 | PF00400 | 0.466 |
DEG_APCC_DBOX_1 | 610 | 618 | PF00400 | 0.501 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.463 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.428 |
DOC_CYCLIN_RxL_1 | 268 | 276 | PF00134 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 454 | 460 | PF00134 | 0.485 |
DOC_MAPK_MEF2A_6 | 602 | 610 | PF00069 | 0.523 |
DOC_MAPK_RevD_3 | 295 | 310 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 110 | 116 | PF00149 | 0.519 |
DOC_PP1_RVXF_1 | 181 | 187 | PF00149 | 0.509 |
DOC_PP1_RVXF_1 | 33 | 40 | PF00149 | 0.455 |
DOC_PP1_RVXF_1 | 618 | 625 | PF00149 | 0.380 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.428 |
DOC_PP2B_LxvP_1 | 458 | 461 | PF13499 | 0.595 |
DOC_PP2B_LxvP_1 | 503 | 506 | PF13499 | 0.520 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.537 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 172 | 177 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 272 | 282 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 493 | 498 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 63 | 69 | PF00244 | 0.553 |
LIG_14-3-3_CterR_2 | 627 | 629 | PF00244 | 0.500 |
LIG_Actin_WH2_2 | 601 | 617 | PF00022 | 0.545 |
LIG_AP2alpha_2 | 103 | 105 | PF02296 | 0.457 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.466 |
LIG_BRCT_BRCA1_1 | 365 | 369 | PF00533 | 0.233 |
LIG_Clathr_ClatBox_1 | 77 | 81 | PF01394 | 0.463 |
LIG_deltaCOP1_diTrp_1 | 178 | 186 | PF00928 | 0.485 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.606 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.439 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.450 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.514 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.510 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.648 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.481 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.448 |
LIG_FHA_2 | 573 | 579 | PF00498 | 0.515 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.488 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.542 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.481 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 533 | 543 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 64 | 72 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 84 | 94 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 540 | 546 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.400 |
LIG_LYPXL_yS_3 | 282 | 285 | PF13949 | 0.388 |
LIG_NRBOX | 241 | 247 | PF00104 | 0.453 |
LIG_NRBOX | 520 | 526 | PF00104 | 0.517 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.460 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.368 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.378 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.421 |
LIG_SH3_1 | 542 | 548 | PF00018 | 0.581 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.435 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.389 |
LIG_SH3_3 | 542 | 548 | PF00018 | 0.581 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.481 |
LIG_SUMO_SIM_anti_2 | 323 | 328 | PF11976 | 0.286 |
LIG_SUMO_SIM_anti_2 | 67 | 73 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 76 | 81 | PF11976 | 0.447 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.509 |
LIG_TRFH_1 | 443 | 447 | PF08558 | 0.545 |
LIG_TYR_ITIM | 227 | 232 | PF00017 | 0.447 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.532 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.684 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.526 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.501 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.791 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.494 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.559 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.693 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.536 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.518 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.491 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.514 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.297 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.501 |
MOD_GlcNHglycan | 157 | 161 | PF01048 | 0.676 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.656 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.364 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.649 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.559 |
MOD_GlcNHglycan | 347 | 351 | PF01048 | 0.528 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.725 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.732 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.580 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.679 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.462 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.721 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.507 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.482 |
MOD_LATS_1 | 170 | 176 | PF00433 | 0.633 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.664 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.541 |
MOD_N-GLC_1 | 391 | 396 | PF02516 | 0.398 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.575 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.610 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.371 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.487 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.383 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.716 |
MOD_NEK2_2 | 143 | 148 | PF00069 | 0.500 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.495 |
MOD_PKA_1 | 493 | 499 | PF00069 | 0.389 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.479 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.389 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.629 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.479 |
MOD_Plk_1 | 486 | 492 | PF00069 | 0.566 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.554 |
MOD_Plk_2-3 | 466 | 472 | PF00069 | 0.550 |
MOD_Plk_2-3 | 579 | 585 | PF00069 | 0.547 |
MOD_Plk_2-3 | 81 | 87 | PF00069 | 0.483 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.469 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.329 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.431 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.379 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.563 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.576 |
TRG_DiLeu_BaEn_1 | 249 | 254 | PF01217 | 0.418 |
TRG_DiLeu_BaEn_2 | 50 | 56 | PF01217 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 270 | 275 | PF01217 | 0.509 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.553 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.511 |
TRG_NES_CRM1_1 | 293 | 305 | PF08389 | 0.428 |
TRG_NES_CRM1_1 | 87 | 100 | PF08389 | 0.278 |
TRG_Pf-PMV_PEXEL_1 | 292 | 296 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 83 | 87 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8B9 | Leptomonas seymouri | 60% | 100% |
A0A0S4JJX6 | Bodo saltans | 34% | 91% |
A0A1X0P2C3 | Trypanosomatidae | 42% | 100% |
A0A3Q8IFL1 | Leishmania donovani | 93% | 100% |
A0A422N122 | Trypanosoma rangeli | 44% | 100% |
A4HHW1 | Leishmania braziliensis | 79% | 100% |
A4I511 | Leishmania infantum | 93% | 100% |
C9ZQG5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B0E1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5AWY0 | Trypanosoma cruzi | 44% | 100% |