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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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: A0A3S7XBL2
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:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018026 | peptidyl-lysine monomethylation | 6 | 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: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 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
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 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.381 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.389 |
CLV_PCSK_PC7_1 | 515 | 521 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.405 |
DOC_CKS1_1 | 434 | 439 | PF01111 | 0.538 |
DOC_MAPK_gen_1 | 27 | 36 | PF00069 | 0.334 |
DOC_MAPK_gen_1 | 395 | 405 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 489 | 496 | PF00069 | 0.338 |
DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.449 |
DOC_PP4_FxxP_1 | 35 | 38 | PF00568 | 0.322 |
DOC_PP4_FxxP_1 | 42 | 45 | PF00568 | 0.315 |
DOC_SPAK_OSR1_1 | 300 | 304 | PF12202 | 0.294 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.449 |
DOC_USP7_UBL2_3 | 27 | 31 | PF12436 | 0.433 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.339 |
LIG_14-3-3_CanoR_1 | 195 | 203 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 269 | 278 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 319 | 325 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 357 | 364 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 415 | 421 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 433 | 437 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 471 | 479 | PF00244 | 0.514 |
LIG_APCC_ABBA_1 | 217 | 222 | PF00400 | 0.449 |
LIG_APCC_ABBA_1 | 34 | 39 | PF00400 | 0.327 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 11 | 15 | PF00533 | 0.455 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 208 | 217 | PF00928 | 0.469 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.543 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.475 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.436 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.511 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.357 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.422 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.448 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.478 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.467 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.467 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.497 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.400 |
LIG_LIR_Apic_2 | 241 | 247 | PF02991 | 0.425 |
LIG_LIR_Apic_2 | 39 | 45 | PF02991 | 0.320 |
LIG_LIR_Apic_2 | 431 | 437 | PF02991 | 0.541 |
LIG_LIR_Apic_2 | 473 | 479 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 273 | 283 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 463 | 472 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 490 | 499 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 216 | 220 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.459 |
LIG_MLH1_MIPbox_1 | 11 | 15 | PF16413 | 0.373 |
LIG_MYND_1 | 243 | 247 | PF01753 | 0.459 |
LIG_PDZ_Class_1 | 537 | 542 | PF00595 | 0.455 |
LIG_Pex14_1 | 373 | 377 | PF04695 | 0.489 |
LIG_Pex14_2 | 228 | 232 | PF04695 | 0.421 |
LIG_Pex14_2 | 301 | 305 | PF04695 | 0.276 |
LIG_PTB_Apo_2 | 250 | 257 | PF02174 | 0.449 |
LIG_Rb_LxCxE_1 | 63 | 83 | PF01857 | 0.529 |
LIG_Rb_pABgroove_1 | 401 | 409 | PF01858 | 0.326 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.463 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.517 |
LIG_SH2_GRB2like | 537 | 540 | PF00017 | 0.371 |
LIG_SH2_NCK_1 | 465 | 469 | PF00017 | 0.389 |
LIG_SH2_SRC | 407 | 410 | PF00017 | 0.479 |
LIG_SH2_SRC | 465 | 468 | PF00017 | 0.316 |
LIG_SH2_SRC | 537 | 540 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 465 | 469 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 537 | 541 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.373 |
LIG_SH3_1 | 79 | 85 | PF00018 | 0.400 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.442 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.516 |
LIG_Sin3_3 | 103 | 110 | PF02671 | 0.420 |
LIG_SUMO_SIM_anti_2 | 104 | 111 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 62 | 67 | PF11976 | 0.512 |
LIG_TRAF2_1 | 439 | 442 | PF00917 | 0.401 |
LIG_WRPW_2 | 119 | 122 | PF00400 | 0.529 |
MOD_CDC14_SPxK_1 | 117 | 120 | PF00782 | 0.449 |
MOD_CDK_SPxK_1 | 114 | 120 | PF00069 | 0.449 |
MOD_CDK_SPxxK_3 | 72 | 79 | PF00069 | 0.449 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.383 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.549 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.448 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.493 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.351 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.495 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.559 |
MOD_CMANNOS | 119 | 122 | PF00535 | 0.236 |
MOD_Cter_Amidation | 267 | 270 | PF01082 | 0.236 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.604 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.362 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.325 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.435 |
MOD_GlcNHglycan | 347 | 351 | PF01048 | 0.547 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.553 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.551 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.481 |
MOD_GlcNHglycan | 6 | 10 | PF01048 | 0.511 |
MOD_GlcNHglycan | 70 | 74 | PF01048 | 0.281 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.684 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.462 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.538 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.541 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.459 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.504 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.406 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.493 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.392 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.436 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.436 |
MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.225 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.580 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.505 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.500 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.381 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.342 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.518 |
MOD_NEK2_2 | 428 | 433 | PF00069 | 0.567 |
MOD_NEK2_2 | 460 | 465 | PF00069 | 0.387 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.538 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.298 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.396 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.534 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.531 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.419 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.441 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.419 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.454 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.554 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.470 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.513 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.432 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.335 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.394 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.425 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.439 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.365 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.460 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.539 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.425 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.425 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.339 |
TRG_DiLeu_BaEn_1 | 241 | 246 | PF01217 | 0.421 |
TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 518 | 520 | PF00400 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 520 | 524 | PF00026 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILW4 | Leptomonas seymouri | 64% | 100% |
A0A0S4J9V9 | Bodo saltans | 34% | 100% |
A0A1X0P0B9 | Trypanosomatidae | 39% | 100% |
A0A3R7KPF2 | Trypanosoma rangeli | 40% | 100% |
A4IE43 | Leishmania infantum | 99% | 100% |
D0A495 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9ATL5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q0Y3 | Leishmania major | 92% | 100% |
V5DLN2 | Trypanosoma cruzi | 41% | 100% |