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:0000118 | histone deacetylase complex | 3 | 2 |
GO:0000812 | Swr1 complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0070603 | SWI/SNF superfamily-type complex | 3 | 2 |
GO:0097346 | INO80-type complex | 4 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1904949 | ATPase complex | 3 | 2 |
GO:0005634 | nucleus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4QCJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 9 |
GO:0006338 | chromatin remodeling | 5 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016043 | cellular component organization | 3 | 9 |
GO:0071840 | cellular component organization or biogenesis | 2 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0031491 | nucleosome binding | 3 | 2 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 474 | 478 | PF00656 | 0.677 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.226 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.226 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.318 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.417 |
CLV_Separin_Metazoa | 548 | 552 | PF03568 | 0.398 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.439 |
DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.458 |
DEG_SPOP_SBC_1 | 160 | 164 | PF00917 | 0.467 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.534 |
DOC_CDC14_PxL_1 | 350 | 358 | PF14671 | 0.439 |
DOC_CKS1_1 | 397 | 402 | PF01111 | 0.518 |
DOC_CYCLIN_RxL_1 | 418 | 428 | PF00134 | 0.486 |
DOC_CYCLIN_yClb3_PxF_3 | 504 | 512 | PF00134 | 0.379 |
DOC_CYCLIN_yCln2_LP_2 | 131 | 137 | PF00134 | 0.481 |
DOC_CYCLIN_yCln2_LP_2 | 18 | 24 | PF00134 | 0.515 |
DOC_CYCLIN_yCln2_LP_2 | 397 | 403 | PF00134 | 0.481 |
DOC_CYCLIN_yCln2_LP_2 | 430 | 436 | PF00134 | 0.486 |
DOC_MAPK_DCC_7 | 390 | 398 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 151 | 160 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 251 | 258 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 390 | 398 | PF00069 | 0.518 |
DOC_PP2B_LxvP_1 | 131 | 134 | PF13499 | 0.457 |
DOC_PP2B_LxvP_1 | 18 | 21 | PF13499 | 0.407 |
DOC_PP2B_LxvP_1 | 61 | 64 | PF13499 | 0.560 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.428 |
DOC_PP4_FxxP_1 | 391 | 394 | PF00568 | 0.425 |
DOC_SPAK_OSR1_1 | 390 | 394 | PF12202 | 0.518 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.528 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.393 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 285 | 289 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 496 | 504 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 571 | 575 | PF00244 | 0.458 |
LIG_APCC_ABBA_1 | 4 | 9 | PF00400 | 0.392 |
LIG_APCC_ABBAyCdc20_2 | 3 | 9 | PF00400 | 0.439 |
LIG_BRCT_BRCA1_1 | 151 | 155 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.396 |
LIG_deltaCOP1_diTrp_1 | 128 | 135 | PF00928 | 0.518 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.440 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.481 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.550 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.487 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.518 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.518 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.434 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.393 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.567 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.518 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.636 |
LIG_LIR_Apic_2 | 389 | 394 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 162 | 173 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 254 | 263 | PF02991 | 0.447 |
LIG_LIR_LC3C_4 | 128 | 133 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.467 |
LIG_MYND_1 | 354 | 358 | PF01753 | 0.439 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.518 |
LIG_NRBOX | 380 | 386 | PF00104 | 0.481 |
LIG_NRBOX | 426 | 432 | PF00104 | 0.486 |
LIG_PCNA_PIPBox_1 | 420 | 429 | PF02747 | 0.486 |
LIG_PCNA_yPIPBox_3 | 571 | 585 | PF02747 | 0.518 |
LIG_PTB_Apo_2 | 7 | 14 | PF02174 | 0.300 |
LIG_PTB_Phospho_1 | 7 | 13 | PF10480 | 0.300 |
LIG_SH2_CRK | 235 | 239 | PF00017 | 0.395 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.481 |
LIG_SH2_GRB2like | 228 | 231 | PF00017 | 0.518 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.449 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.483 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.366 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.456 |
LIG_SH3_1 | 348 | 354 | PF00018 | 0.425 |
LIG_SH3_2 | 342 | 347 | PF14604 | 0.486 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.544 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.361 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.397 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.525 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.504 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.481 |
LIG_SUMO_SIM_anti_2 | 157 | 164 | PF11976 | 0.455 |
LIG_TRAF2_1 | 123 | 126 | PF00917 | 0.486 |
LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.486 |
LIG_UBA3_1 | 423 | 429 | PF00899 | 0.449 |
LIG_WRC_WIRS_1 | 255 | 260 | PF05994 | 0.457 |
LIG_WRC_WIRS_1 | 574 | 579 | PF05994 | 0.464 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.449 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.481 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.481 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.553 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.358 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.592 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.561 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.448 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.724 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.463 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.412 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.635 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.567 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.487 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.349 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.262 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.310 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.522 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.163 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.597 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.254 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.610 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.318 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.394 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.431 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.570 |
MOD_GlcNHglycan | 558 | 562 | PF01048 | 0.473 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.457 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.535 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.502 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.505 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.527 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.648 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.748 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.397 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.530 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.512 |
MOD_N-GLC_2 | 438 | 440 | PF02516 | 0.286 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.510 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.450 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.697 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.735 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.351 |
MOD_NEK2_2 | 149 | 154 | PF00069 | 0.518 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.375 |
MOD_OFUCOSY | 493 | 499 | PF10250 | 0.493 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.463 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.467 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.486 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.451 |
MOD_PK_1 | 154 | 160 | PF00069 | 0.465 |
MOD_PKA_1 | 479 | 485 | PF00069 | 0.604 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.449 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.486 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.711 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.294 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.514 |
MOD_PKB_1 | 185 | 193 | PF00069 | 0.449 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.481 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.492 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.425 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.425 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.439 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.439 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.498 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.537 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.519 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.481 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.567 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.389 |
MOD_SUMO_rev_2 | 468 | 478 | PF00179 | 0.582 |
TRG_DiLeu_BaEn_1 | 265 | 270 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 430 | 435 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 521 | 526 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 550 | 553 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.426 |
TRG_NLS_MonoCore_2 | 185 | 190 | PF00514 | 0.486 |
TRG_NLS_MonoExtC_3 | 184 | 189 | PF00514 | 0.518 |
TRG_NLS_MonoExtN_4 | 185 | 190 | PF00514 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 390 | 395 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.283 |
TRG_Pf-PMV_PEXEL_1 | 553 | 558 | PF00026 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4I4 | Leptomonas seymouri | 53% | 93% |
A0A0S4IXC8 | Bodo saltans | 35% | 100% |
A0A3R7KCE3 | Trypanosoma rangeli | 38% | 100% |
A0A3S7WWF5 | Leishmania donovani | 94% | 99% |
A4HBM2 | Leishmania braziliensis | 78% | 98% |
A4HZB0 | Leishmania infantum | 93% | 99% |
D0A1L4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AUZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 98% |
O94241 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
P0CM04 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 24% | 100% |
P0CM05 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 24% | 100% |
P45890 | Drosophila melanogaster | 26% | 100% |
Q09443 | Caenorhabditis elegans | 27% | 100% |
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% |
Q6BML9 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 21% | 100% |
Q6CJF4 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 23% | 100% |
Q74ZV8 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 24% | 100% |
Q7S6X6 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 26% | 100% |
Q8LGE3 | Arabidopsis thaliana | 26% | 100% |
Q9D864 | Mus musculus | 25% | 100% |
Q9DEE9 | Gallus gallus | 25% | 100% |
Q9GZN1 | Homo sapiens | 25% | 100% |
V5B0N4 | Trypanosoma cruzi | 43% | 100% |