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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
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 |
Related structures:
AlphaFold database: E9ANP2
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 | 140 | 144 | PF00656 | 0.710 |
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.644 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.818 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.739 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.800 |
CLV_PCSK_FUR_1 | 402 | 406 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.720 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.780 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.706 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.803 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.802 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.436 |
DEG_APCC_KENBOX_2 | 408 | 412 | PF00400 | 0.638 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.585 |
DEG_SPOP_SBC_1 | 293 | 297 | PF00917 | 0.702 |
DOC_ANK_TNKS_1 | 206 | 213 | PF00023 | 0.692 |
DOC_CYCLIN_RxL_1 | 473 | 482 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 257 | 264 | PF00069 | 0.657 |
DOC_PP1_RVXF_1 | 475 | 482 | PF00149 | 0.548 |
DOC_PP4_FxxP_1 | 392 | 395 | PF00568 | 0.577 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.786 |
DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.715 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.828 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.608 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.725 |
LIG_14-3-3_CanoR_1 | 19 | 27 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 300 | 307 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 352 | 360 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 367 | 371 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 458 | 467 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 91 | 98 | PF00244 | 0.754 |
LIG_Actin_WH2_2 | 464 | 482 | PF00022 | 0.611 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.570 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.684 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.588 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.524 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.574 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.798 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.714 |
LIG_GBD_Chelix_1 | 254 | 262 | PF00786 | 0.539 |
LIG_LIR_Apic_2 | 426 | 430 | PF02991 | 0.783 |
LIG_LIR_Apic_2 | 49 | 55 | PF02991 | 0.711 |
LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 249 | 258 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 336 | 345 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 461 | 472 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 336 | 340 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 453 | 457 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.486 |
LIG_PDZ_Class_2 | 478 | 483 | PF00595 | 0.572 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.402 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.546 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.538 |
LIG_SH2_SRC | 313 | 316 | PF00017 | 0.711 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.788 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.657 |
LIG_SUMO_SIM_par_1 | 197 | 204 | PF11976 | 0.822 |
LIG_TRAF2_1 | 355 | 358 | PF00917 | 0.801 |
LIG_TRFH_1 | 331 | 335 | PF08558 | 0.649 |
LIG_WRC_WIRS_1 | 304 | 309 | PF05994 | 0.504 |
MOD_CDK_SPxxK_3 | 282 | 289 | PF00069 | 0.765 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.576 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.830 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.741 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.716 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.612 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.673 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.809 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.571 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.747 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.667 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.801 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.728 |
MOD_GlcNHglycan | 137 | 142 | PF01048 | 0.676 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.685 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.747 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.692 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.666 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.633 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.805 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.713 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.602 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.673 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.643 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.684 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.762 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.748 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.826 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.695 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.517 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.626 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.763 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.684 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.686 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.799 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.739 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.559 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.704 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.711 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.770 |
MOD_NEK2_2 | 116 | 121 | PF00069 | 0.541 |
MOD_NEK2_2 | 381 | 386 | PF00069 | 0.605 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.789 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.720 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.811 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.713 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.780 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.674 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.667 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.552 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.669 |
MOD_Plk_2-3 | 429 | 435 | PF00069 | 0.686 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.576 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.696 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.537 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.724 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.701 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.658 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.722 |
MOD_SUMO_for_1 | 258 | 261 | PF00179 | 0.656 |
MOD_SUMO_rev_2 | 143 | 152 | PF00179 | 0.796 |
MOD_SUMO_rev_2 | 232 | 239 | PF00179 | 0.727 |
MOD_SUMO_rev_2 | 308 | 314 | PF00179 | 0.733 |
TRG_DiLeu_BaEn_2 | 21 | 27 | PF01217 | 0.633 |
TRG_DiLeu_BaLyEn_6 | 323 | 328 | PF01217 | 0.665 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.709 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.546 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.825 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 457 | 460 | PF00400 | 0.541 |
TRG_NLS_Bipartite_1 | 206 | 222 | PF00514 | 0.822 |
TRG_NLS_MonoCore_2 | 217 | 222 | PF00514 | 0.827 |
TRG_NLS_MonoCore_2 | 401 | 406 | PF00514 | 0.800 |
TRG_NLS_MonoExtC_3 | 216 | 221 | PF00514 | 0.827 |
TRG_NLS_MonoExtC_3 | 402 | 407 | PF00514 | 0.806 |
TRG_NLS_MonoExtN_4 | 217 | 222 | PF00514 | 0.823 |
TRG_NLS_MonoExtN_4 | 402 | 407 | PF00514 | 0.806 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYI9 | Leptomonas seymouri | 38% | 91% |
A0A3Q8I947 | Leishmania donovani | 88% | 100% |
A4H6M4 | Leishmania braziliensis | 76% | 100% |
A4HV07 | Leishmania infantum | 88% | 100% |
Q4QGY1 | Leishmania major | 87% | 100% |