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: 5 |
NetGPI | no | yes: 0, no: 5 |
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 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: Q4QGY1
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 | 141 | 145 | PF00656 | 0.597 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.755 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.638 |
CLV_PCSK_FUR_1 | 403 | 407 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.754 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.765 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 83 | 85 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.388 |
DEG_SCF_TRCP1_1 | 413 | 418 | PF00400 | 0.613 |
DEG_SPOP_SBC_1 | 296 | 300 | PF00917 | 0.684 |
DEG_SPOP_SBC_1 | 372 | 376 | PF00917 | 0.549 |
DOC_ANK_TNKS_1 | 207 | 214 | PF00023 | 0.630 |
DOC_CYCLIN_RxL_1 | 474 | 483 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 258 | 265 | PF00069 | 0.516 |
DOC_PP1_RVXF_1 | 476 | 483 | PF00149 | 0.548 |
DOC_PP4_FxxP_1 | 393 | 396 | PF00568 | 0.544 |
DOC_PP4_FxxP_1 | 428 | 431 | PF00568 | 0.639 |
DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.597 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.512 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 19 | 27 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 301 | 308 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 353 | 361 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 368 | 372 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 459 | 468 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 92 | 99 | PF00244 | 0.625 |
LIG_Actin_WH2_2 | 465 | 483 | PF00022 | 0.607 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.593 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.532 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.544 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.463 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.552 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.589 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.532 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.667 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.636 |
LIG_GBD_Chelix_1 | 255 | 263 | PF00786 | 0.475 |
LIG_LIR_Apic_2 | 392 | 396 | PF02991 | 0.520 |
LIG_LIR_Apic_2 | 427 | 431 | PF02991 | 0.637 |
LIG_LIR_Apic_2 | 49 | 55 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 337 | 346 | PF02991 | 0.765 |
LIG_LIR_Gen_1 | 462 | 473 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 337 | 341 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 454 | 458 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 462 | 468 | PF02991 | 0.479 |
LIG_PDZ_Class_2 | 479 | 484 | PF00595 | 0.567 |
LIG_SH2_CRK | 455 | 459 | PF00017 | 0.532 |
LIG_SH2_SRC | 117 | 120 | PF00017 | 0.507 |
LIG_SH2_SRC | 314 | 317 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.795 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.575 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.672 |
LIG_SUMO_SIM_par_1 | 198 | 205 | PF11976 | 0.681 |
LIG_TRAF2_1 | 356 | 359 | PF00917 | 0.666 |
LIG_TRFH_1 | 332 | 336 | PF08558 | 0.631 |
MOD_CDK_SPxxK_3 | 283 | 290 | PF00069 | 0.635 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.514 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.780 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.711 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.656 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.582 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.555 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.541 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.589 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.604 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.529 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.700 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.650 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.435 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.621 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.567 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.659 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.607 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.660 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.645 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.666 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.776 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.753 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.583 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.537 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.582 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.739 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.648 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.602 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.670 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.572 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.634 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.551 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.634 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.697 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.638 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.463 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.620 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.681 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.708 |
MOD_NEK2_2 | 117 | 122 | PF00069 | 0.510 |
MOD_NEK2_2 | 382 | 387 | PF00069 | 0.493 |
MOD_PKA_1 | 404 | 410 | PF00069 | 0.622 |
MOD_PKA_1 | 88 | 94 | PF00069 | 0.656 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.538 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.686 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.734 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.688 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.622 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.631 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.529 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.589 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.548 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.714 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.631 |
MOD_SUMO_for_1 | 259 | 262 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 144 | 153 | PF00179 | 0.653 |
MOD_SUMO_rev_2 | 235 | 240 | PF00179 | 0.629 |
MOD_SUMO_rev_2 | 309 | 315 | PF00179 | 0.636 |
TRG_DiLeu_BaEn_2 | 21 | 27 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 324 | 329 | PF01217 | 0.635 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.777 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.532 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 403 | 406 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 458 | 461 | PF00400 | 0.532 |
TRG_NLS_Bipartite_1 | 207 | 223 | PF00514 | 0.678 |
TRG_NLS_MonoCore_2 | 218 | 223 | PF00514 | 0.682 |
TRG_NLS_MonoCore_2 | 402 | 407 | PF00514 | 0.680 |
TRG_NLS_MonoExtC_3 | 217 | 222 | PF00514 | 0.681 |
TRG_NLS_MonoExtC_3 | 403 | 408 | PF00514 | 0.686 |
TRG_NLS_MonoExtN_4 | 169 | 175 | PF00514 | 0.557 |
TRG_NLS_MonoExtN_4 | 218 | 223 | PF00514 | 0.680 |
TRG_NLS_MonoExtN_4 | 403 | 408 | PF00514 | 0.686 |
TRG_Pf-PMV_PEXEL_1 | 208 | 212 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I947 | Leishmania donovani | 92% | 100% |
A4H6M4 | Leishmania braziliensis | 73% | 100% |
A4HV07 | Leishmania infantum | 92% | 100% |
E9ANP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |