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 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000118 | histone deacetylase complex | 3 | 1 |
GO:0000812 | Swr1 complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0070603 | SWI/SNF superfamily-type complex | 3 | 1 |
GO:0097346 | INO80-type complex | 4 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1904949 | ATPase complex | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AUZ0
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 10 |
GO:0006338 | chromatin remodeling | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0031491 | nucleosome binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 373 | 377 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.671 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.214 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.214 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.396 |
CLV_Separin_Metazoa | 561 | 565 | PF03568 | 0.378 |
DEG_APCC_DBOX_1 | 345 | 353 | PF00400 | 0.427 |
DEG_APCC_DBOX_1 | 419 | 427 | PF00400 | 0.446 |
DEG_SPOP_SBC_1 | 160 | 164 | PF00917 | 0.445 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.486 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.499 |
DOC_CDC14_PxL_1 | 349 | 357 | PF14671 | 0.427 |
DOC_CKS1_1 | 396 | 401 | PF01111 | 0.509 |
DOC_CYCLIN_RxL_1 | 417 | 427 | PF00134 | 0.460 |
DOC_CYCLIN_yClb3_PxF_3 | 507 | 515 | PF00134 | 0.366 |
DOC_CYCLIN_yCln2_LP_2 | 131 | 137 | PF00134 | 0.470 |
DOC_CYCLIN_yCln2_LP_2 | 18 | 24 | PF00134 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 396 | 402 | PF00134 | 0.470 |
DOC_CYCLIN_yCln2_LP_2 | 429 | 435 | PF00134 | 0.460 |
DOC_MAPK_DCC_7 | 389 | 397 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 151 | 160 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 251 | 258 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 329 | 337 | PF00069 | 0.343 |
DOC_MAPK_MEF2A_6 | 389 | 397 | PF00069 | 0.509 |
DOC_PP2B_LxvP_1 | 131 | 134 | PF13499 | 0.445 |
DOC_PP2B_LxvP_1 | 18 | 21 | PF13499 | 0.356 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.418 |
DOC_PP2B_LxvP_1 | 61 | 64 | PF13499 | 0.460 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.417 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.414 |
DOC_SPAK_OSR1_1 | 389 | 393 | PF12202 | 0.509 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.384 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 285 | 289 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 499 | 507 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 584 | 588 | PF00244 | 0.432 |
LIG_APCC_ABBA_1 | 4 | 9 | PF00400 | 0.345 |
LIG_APCC_ABBAyCdc20_2 | 3 | 9 | PF00400 | 0.423 |
LIG_BRCT_BRCA1_1 | 151 | 155 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.387 |
LIG_deltaCOP1_diTrp_1 | 128 | 135 | PF00928 | 0.509 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.429 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.470 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.470 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.491 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.509 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.490 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.366 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.390 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.564 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.509 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.598 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.482 |
LIG_FHA_2 | 536 | 542 | PF00498 | 0.525 |
LIG_LIR_Apic_2 | 132 | 138 | PF02991 | 0.398 |
LIG_LIR_Apic_2 | 388 | 393 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 162 | 173 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 254 | 263 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.460 |
LIG_MYND_1 | 353 | 357 | PF01753 | 0.427 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.509 |
LIG_NRBOX | 379 | 385 | PF00104 | 0.470 |
LIG_NRBOX | 425 | 431 | PF00104 | 0.460 |
LIG_PCNA_PIPBox_1 | 419 | 428 | PF02747 | 0.460 |
LIG_PCNA_yPIPBox_3 | 584 | 598 | PF02747 | 0.497 |
LIG_PTB_Apo_2 | 7 | 14 | PF02174 | 0.282 |
LIG_PTB_Phospho_1 | 7 | 13 | PF10480 | 0.282 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.470 |
LIG_SH2_GRB2like | 228 | 231 | PF00017 | 0.509 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.429 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.468 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.427 |
LIG_SH3_1 | 347 | 353 | PF00018 | 0.414 |
LIG_SH3_2 | 341 | 346 | PF14604 | 0.460 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.538 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.355 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.388 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.517 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.509 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.470 |
LIG_SUMO_SIM_anti_2 | 157 | 164 | PF11976 | 0.444 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.460 |
LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.460 |
LIG_UBA3_1 | 422 | 428 | PF00899 | 0.429 |
LIG_WRC_WIRS_1 | 255 | 260 | PF05994 | 0.445 |
LIG_WRC_WIRS_1 | 587 | 592 | PF05994 | 0.445 |
MOD_CDK_SPK_2 | 321 | 326 | PF00069 | 0.390 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.429 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.499 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.513 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.536 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.348 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.559 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.539 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.438 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.698 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.768 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.451 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.596 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.559 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.472 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.343 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.240 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.279 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.470 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.148 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.525 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.508 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.309 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.397 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.600 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.443 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.445 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.445 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.481 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.513 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.622 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.747 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.408 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.508 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.522 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.460 |
MOD_N-GLC_2 | 437 | 439 | PF02516 | 0.260 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.491 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.455 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.420 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.471 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.591 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.405 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.332 |
MOD_NEK2_2 | 149 | 154 | PF00069 | 0.509 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.427 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.404 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.460 |
MOD_PIKK_1 | 555 | 561 | PF00454 | 0.426 |
MOD_PK_1 | 154 | 160 | PF00069 | 0.453 |
MOD_PKA_1 | 478 | 484 | PF00069 | 0.584 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.429 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.470 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.680 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.312 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.488 |
MOD_PKB_1 | 185 | 193 | PF00069 | 0.429 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.470 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.451 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.414 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.414 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.427 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.427 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.500 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.491 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.510 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.470 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.380 |
MOD_SUMO_rev_2 | 469 | 477 | PF00179 | 0.553 |
TRG_DiLeu_BaEn_1 | 265 | 270 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 429 | 434 | PF01217 | 0.560 |
TRG_DiLeu_BaLyEn_6 | 524 | 529 | PF01217 | 0.420 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 563 | 566 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.414 |
TRG_NLS_MonoCore_2 | 185 | 190 | PF00514 | 0.460 |
TRG_NLS_MonoExtC_3 | 184 | 189 | PF00514 | 0.509 |
TRG_NLS_MonoExtN_4 | 185 | 190 | PF00514 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 389 | 394 | PF00026 | 0.309 |
TRG_Pf-PMV_PEXEL_1 | 420 | 424 | PF00026 | 0.272 |
TRG_Pf-PMV_PEXEL_1 | 566 | 571 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4I4 | Leptomonas seymouri | 51% | 95% |
A0A0S4IXC8 | Bodo saltans | 34% | 100% |
A0A3R7KCE3 | Trypanosoma rangeli | 41% | 100% |
A0A3S7WWF5 | Leishmania donovani | 92% | 100% |
A2WNB0 | Oryza sativa subsp. indica | 28% | 100% |
A4HBM2 | Leishmania braziliensis | 79% | 99% |
A4HZB0 | Leishmania infantum | 91% | 100% |
D0A1L4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
O94241 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
P0CM04 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 25% | 100% |
P0CM05 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 25% | 100% |
Q09443 | Caenorhabditis elegans | 27% | 100% |
Q4QCJ2 | Leishmania major | 91% | 98% |
Q4W9M3 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 100% |
Q5AXH1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 27% | 100% |
Q5NBI2 | Oryza sativa subsp. japonica | 28% | 100% |
Q6CJF4 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 22% | 100% |
Q74ZV8 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 23% | 100% |
Q7S6X6 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 100% |
V5B0N4 | Trypanosoma cruzi | 41% | 100% |