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:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HDF7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007131 | reciprocal meiotic recombination | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0035825 | homologous recombination | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0140527 | reciprocal homologous recombination | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.613 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.637 |
CLV_PCSK_FUR_1 | 423 | 427 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 415 | 417 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.645 |
CLV_PCSK_PC7_1 | 416 | 422 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.537 |
CLV_Separin_Metazoa | 122 | 126 | PF03568 | 0.427 |
DEG_SCF_FBW7_1 | 319 | 326 | PF00400 | 0.562 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.363 |
DOC_CKS1_1 | 320 | 325 | PF01111 | 0.563 |
DOC_CYCLIN_yCln2_LP_2 | 283 | 289 | PF00134 | 0.544 |
DOC_MAPK_gen_1 | 276 | 287 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 420 | 429 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 8 | 17 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 280 | 289 | PF00069 | 0.536 |
DOC_MAPK_NFAT4_5 | 280 | 288 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 178 | 184 | PF00149 | 0.505 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.462 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.750 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.661 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.312 |
LIG_14-3-3_CanoR_1 | 169 | 175 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 254 | 261 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 346 | 356 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 72 | 82 | PF00244 | 0.312 |
LIG_14-3-3_CterR_2 | 425 | 429 | PF00244 | 0.628 |
LIG_CtBP_PxDLS_1 | 286 | 290 | PF00389 | 0.551 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.400 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.677 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.312 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.314 |
LIG_Integrin_RGD_1 | 374 | 376 | PF01839 | 0.555 |
LIG_LIR_Apic_2 | 77 | 83 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 145 | 154 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 158 | 162 | PF02991 | 0.381 |
LIG_MYND_1 | 331 | 335 | PF01753 | 0.558 |
LIG_PDZ_Class_2 | 424 | 429 | PF00595 | 0.532 |
LIG_Pex14_1 | 255 | 259 | PF04695 | 0.417 |
LIG_PTAP_UEV_1 | 385 | 390 | PF05743 | 0.548 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.312 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.668 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.728 |
LIG_SUMO_SIM_par_1 | 285 | 290 | PF11976 | 0.544 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.508 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.533 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.316 |
LIG_TYR_ITIM | 50 | 55 | PF00017 | 0.312 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.560 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.607 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.569 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.593 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.446 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.522 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.418 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.612 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.189 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.536 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.312 |
MOD_Cter_Amidation | 10 | 13 | PF01082 | 0.649 |
MOD_Cter_Amidation | 418 | 421 | PF01082 | 0.713 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.644 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.497 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.436 |
MOD_GlcNHglycan | 185 | 189 | PF01048 | 0.704 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.557 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.559 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.605 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.633 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.707 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.624 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.455 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.424 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.619 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.604 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.597 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.601 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.699 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.660 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.590 |
MOD_LATS_1 | 31 | 37 | PF00433 | 0.231 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.430 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.549 |
MOD_N-GLC_2 | 340 | 342 | PF02516 | 0.727 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.539 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.786 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.647 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.572 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.393 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.588 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.606 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.627 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.555 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.620 |
MOD_PK_1 | 13 | 19 | PF00069 | 0.536 |
MOD_PK_1 | 243 | 249 | PF00069 | 0.356 |
MOD_PKA_1 | 125 | 131 | PF00069 | 0.467 |
MOD_PKA_1 | 415 | 421 | PF00069 | 0.638 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.467 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.514 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.359 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.638 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.375 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.549 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.549 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.599 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.312 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.518 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.752 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.312 |
MOD_SUMO_rev_2 | 16 | 22 | PF00179 | 0.433 |
TRG_DiLeu_BaEn_1 | 19 | 24 | PF01217 | 0.387 |
TRG_DiLeu_BaEn_1 | 352 | 357 | PF01217 | 0.540 |
TRG_DiLeu_BaEn_1 | 39 | 44 | PF01217 | 0.243 |
TRG_DiLeu_BaEn_1 | 57 | 62 | PF01217 | 0.312 |
TRG_DiLeu_BaEn_2 | 178 | 184 | PF01217 | 0.577 |
TRG_DiLeu_BaEn_4 | 176 | 182 | PF01217 | 0.399 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.312 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.564 |
TRG_NLS_MonoExtC_3 | 7 | 12 | PF00514 | 0.672 |
TRG_NLS_MonoExtN_4 | 8 | 13 | PF00514 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBI5 | Leptomonas seymouri | 49% | 100% |
A0A3S7WY90 | Leishmania donovani | 73% | 100% |
A4I0T8 | Leishmania infantum | 73% | 100% |
E9AWU2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4QAN2 | Leishmania major | 73% | 100% |