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 | 1 |
GO:0009295 | nucleoid | 2 | 1 |
GO:0042645 | mitochondrial nucleoid | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HER3
Term | Name | Level | Count |
---|---|---|---|
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006301 | postreplication repair | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019985 | translesion synthesis | 7 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0070987 | error-free translesion synthesis | 8 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071897 | DNA biosynthetic process | 5 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 573 | 577 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.517 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 439 | 441 | PF00082 | 0.513 |
CLV_PCSK_PC7_1 | 178 | 184 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.500 |
CLV_Separin_Metazoa | 336 | 340 | PF03568 | 0.600 |
DEG_APCC_DBOX_1 | 330 | 338 | PF00400 | 0.511 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.407 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.590 |
DOC_MAPK_MEF2A_6 | 497 | 504 | PF00069 | 0.411 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.615 |
DOC_PP4_FxxP_1 | 589 | 592 | PF00568 | 0.571 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.499 |
DOC_SPAK_OSR1_1 | 205 | 209 | PF12202 | 0.607 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.619 |
DOC_USP7_MATH_2 | 279 | 285 | PF00917 | 0.591 |
DOC_USP7_UBL2_3 | 17 | 21 | PF12436 | 0.413 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 522 | 526 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 75 | 83 | PF00244 | 0.514 |
LIG_Actin_WH2_2 | 48 | 63 | PF00022 | 0.488 |
LIG_Actin_WH2_2 | 76 | 92 | PF00022 | 0.626 |
LIG_APCC_ABBA_1 | 502 | 507 | PF00400 | 0.502 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.763 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 479 | 483 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 76 | 80 | PF00533 | 0.520 |
LIG_Clathr_ClatBox_1 | 450 | 454 | PF01394 | 0.411 |
LIG_CtBP_PxDLS_1 | 196 | 200 | PF00389 | 0.632 |
LIG_EVH1_2 | 202 | 206 | PF00568 | 0.612 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.541 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.681 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.447 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.666 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.476 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.467 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.650 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.496 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.481 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.585 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.500 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.563 |
LIG_LIR_Apic_2 | 19 | 25 | PF02991 | 0.537 |
LIG_LIR_Apic_2 | 57 | 62 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 77 | 86 | PF02991 | 0.516 |
LIG_LIR_LC3C_4 | 447 | 452 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.516 |
LIG_MYND_1 | 473 | 477 | PF01753 | 0.411 |
LIG_PTB_Apo_2 | 41 | 48 | PF02174 | 0.576 |
LIG_PTB_Phospho_1 | 41 | 47 | PF10480 | 0.574 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 22 | 26 | PF00017 | 0.540 |
LIG_SH2_PTP2 | 426 | 429 | PF00017 | 0.411 |
LIG_SH2_SRC | 22 | 25 | PF00017 | 0.541 |
LIG_SH2_SRC | 426 | 429 | PF00017 | 0.411 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.355 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.758 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.627 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.621 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.560 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.590 |
LIG_SUMO_SIM_par_1 | 213 | 221 | PF11976 | 0.657 |
LIG_SUMO_SIM_par_1 | 228 | 235 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 449 | 455 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 523 | 529 | PF11976 | 0.560 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.565 |
LIG_TRAF2_1 | 539 | 542 | PF00917 | 0.616 |
LIG_TYR_ITIM | 424 | 429 | PF00017 | 0.411 |
MOD_CDK_SPxK_1 | 389 | 395 | PF00069 | 0.650 |
MOD_CDK_SPxxK_3 | 389 | 396 | PF00069 | 0.506 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.771 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.613 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.775 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.479 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.590 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.445 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.657 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.672 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.411 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.525 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.632 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.509 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.411 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.572 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.513 |
MOD_Cter_Amidation | 14 | 17 | PF01082 | 0.395 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.723 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.786 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.454 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.660 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.675 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.681 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.261 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.411 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.411 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.489 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.704 |
MOD_GlcNHglycan | 549 | 553 | PF01048 | 0.753 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.615 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.516 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.641 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.793 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.688 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.337 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.525 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.648 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.500 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.630 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.734 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.386 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.469 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.611 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.614 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.527 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.641 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.744 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.626 |
MOD_N-GLC_1 | 587 | 592 | PF02516 | 0.576 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.450 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.646 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.513 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.657 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.654 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.399 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.483 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.457 |
MOD_PK_1 | 403 | 409 | PF00069 | 0.571 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.411 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.623 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.657 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.774 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.411 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.454 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.519 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.518 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.620 |
MOD_Plk_2-3 | 272 | 278 | PF00069 | 0.793 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.623 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.725 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.479 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.357 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.698 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.709 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.788 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.650 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.633 |
MOD_SUMO_rev_2 | 121 | 129 | PF00179 | 0.570 |
MOD_SUMO_rev_2 | 275 | 285 | PF00179 | 0.588 |
MOD_SUMO_rev_2 | 412 | 420 | PF00179 | 0.397 |
TRG_DiLeu_BaEn_1 | 165 | 170 | PF01217 | 0.613 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.622 |
TRG_DiLeu_BaEn_1 | 333 | 338 | PF01217 | 0.637 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.609 |
TRG_ER_diLys_1 | 591 | 596 | PF00400 | 0.827 |
TRG_NES_CRM1_1 | 27 | 41 | PF08389 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I464 | Leptomonas seymouri | 52% | 100% |
A0A3Q8IGW6 | Leishmania donovani | 80% | 100% |
A4I1Z0 | Leishmania infantum | 81% | 100% |
E9AY37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q9D6 | Leishmania major | 79% | 97% |