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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
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: E9AW97
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 |
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: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 | 138 | 142 | PF00656 | 0.496 |
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.474 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.461 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.448 |
DEG_SPOP_SBC_1 | 222 | 226 | PF00917 | 0.507 |
DOC_CKS1_1 | 119 | 124 | PF01111 | 0.394 |
DOC_CKS1_1 | 294 | 299 | PF01111 | 0.444 |
DOC_CYCLIN_RxL_1 | 320 | 328 | PF00134 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 119 | 125 | PF00134 | 0.416 |
DOC_MAPK_gen_1 | 453 | 463 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 181 | 189 | PF00069 | 0.221 |
DOC_PP1_RVXF_1 | 235 | 242 | PF00149 | 0.316 |
DOC_PP4_FxxP_1 | 167 | 170 | PF00568 | 0.329 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.381 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.267 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.423 |
DOC_USP7_MATH_2 | 403 | 409 | PF00917 | 0.614 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 245 | 249 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 329 | 336 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.402 |
LIG_Actin_WH2_2 | 434 | 452 | PF00022 | 0.478 |
LIG_APCC_ABBA_1 | 100 | 105 | PF00400 | 0.349 |
LIG_BRCT_BRCA1_1 | 119 | 123 | PF00533 | 0.404 |
LIG_BRCT_BRCA1_1 | 408 | 412 | PF00533 | 0.399 |
LIG_EVH1_2 | 41 | 45 | PF00568 | 0.337 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.607 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.397 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.347 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.541 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.476 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.373 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.446 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.477 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.477 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.426 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.534 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.595 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.558 |
LIG_Integrin_RGD_1 | 277 | 279 | PF01839 | 0.411 |
LIG_LIR_Apic_2 | 110 | 114 | PF02991 | 0.367 |
LIG_LIR_Apic_2 | 165 | 170 | PF02991 | 0.326 |
LIG_LIR_Apic_2 | 398 | 402 | PF02991 | 0.542 |
LIG_LIR_Apic_2 | 44 | 48 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 285 | 295 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 409 | 419 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 309 | 313 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 464 | 468 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 69 | 74 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.407 |
LIG_NRBOX | 321 | 327 | PF00104 | 0.511 |
LIG_NRBOX | 420 | 426 | PF00104 | 0.535 |
LIG_PCNA_PIPBox_1 | 479 | 488 | PF02747 | 0.449 |
LIG_PCNA_yPIPBox_3 | 475 | 486 | PF02747 | 0.436 |
LIG_PDZ_Class_3 | 505 | 510 | PF00595 | 0.416 |
LIG_PTB_Apo_2 | 481 | 488 | PF02174 | 0.502 |
LIG_SH2_CRK | 422 | 426 | PF00017 | 0.535 |
LIG_SH2_PTP2 | 399 | 402 | PF00017 | 0.491 |
LIG_SH2_PTP2 | 465 | 468 | PF00017 | 0.376 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 485 | 488 | PF00017 | 0.388 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.323 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.379 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.485 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.498 |
LIG_SUMO_SIM_par_1 | 115 | 121 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 459 | 464 | PF11976 | 0.493 |
LIG_TRFH_1 | 399 | 403 | PF08558 | 0.507 |
LIG_TYR_ITIM | 463 | 468 | PF00017 | 0.503 |
MOD_CDK_SPxxK_3 | 293 | 300 | PF00069 | 0.282 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.405 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.744 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.698 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.373 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.412 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.556 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.496 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.468 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.522 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.565 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.517 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.479 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.480 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.520 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.704 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.646 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.755 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.690 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.501 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.261 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.179 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.490 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.624 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.353 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.754 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.633 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.387 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.382 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.416 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.445 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.384 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.592 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.231 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.453 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.428 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.535 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.381 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.473 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.344 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.485 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.405 |
MOD_NEK2_2 | 485 | 490 | PF00069 | 0.380 |
MOD_OFUCOSY | 427 | 432 | PF10250 | 0.278 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.371 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.582 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.500 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.318 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.447 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.413 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.467 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.444 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.419 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.522 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.458 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.364 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.451 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.421 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.407 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.414 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.482 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.515 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.493 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.552 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.695 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.334 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.447 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.465 |
MOD_SUMO_rev_2 | 84 | 90 | PF00179 | 0.428 |
TRG_DiLeu_BaLyEn_6 | 178 | 183 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.362 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.425 |
TRG_NES_CRM1_1 | 66 | 79 | PF08389 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 323 | 328 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 383 | 388 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL96 | Leptomonas seymouri | 56% | 100% |
A0A0S4IN59 | Bodo saltans | 31% | 100% |
A0A1X0NWW3 | Trypanosomatidae | 38% | 100% |
A0A3Q8IBR8 | Leishmania donovani | 89% | 100% |
A0A422N8X4 | Trypanosoma rangeli | 39% | 100% |
A4HCV2 | Leishmania braziliensis | 75% | 99% |
A4I0D3 | Leishmania infantum | 89% | 100% |
C9ZV37 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
Q4QB81 | Leishmania major | 87% | 100% |
V5BBM7 | Trypanosoma cruzi | 38% | 100% |