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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
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: E9AWU2
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 | 297 | 301 | PF00656 | 0.643 |
CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.718 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.720 |
CLV_PCSK_PC1ET2_1 | 418 | 420 | PF00082 | 0.749 |
CLV_PCSK_PC1ET2_1 | 423 | 425 | PF00082 | 0.732 |
CLV_PCSK_PC7_1 | 419 | 425 | PF00082 | 0.741 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.721 |
CLV_Separin_Metazoa | 123 | 127 | PF03568 | 0.532 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.550 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.544 |
DEG_SCF_FBW7_1 | 386 | 392 | PF00400 | 0.504 |
DOC_CKS1_1 | 386 | 391 | PF01111 | 0.504 |
DOC_CYCLIN_yCln2_LP_2 | 286 | 292 | PF00134 | 0.574 |
DOC_MAPK_gen_1 | 279 | 290 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 283 | 292 | PF00069 | 0.581 |
DOC_MAPK_NFAT4_5 | 283 | 291 | PF00069 | 0.571 |
DOC_PP1_RVXF_1 | 181 | 187 | PF00149 | 0.608 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.488 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.687 |
DOC_USP7_UBL2_3 | 10 | 14 | PF12436 | 0.687 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.378 |
LIG_14-3-3_CanoR_1 | 172 | 178 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 257 | 264 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 349 | 358 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 73 | 83 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 93 | 97 | PF00244 | 0.445 |
LIG_14-3-3_CterR_2 | 424 | 427 | PF00244 | 0.806 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.723 |
LIG_BIR_III_2 | 329 | 333 | PF00653 | 0.625 |
LIG_BIR_III_2 | 367 | 371 | PF00653 | 0.685 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.459 |
LIG_CtBP_PxDLS_1 | 289 | 293 | PF00389 | 0.646 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.360 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.307 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.307 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.507 |
LIG_LIR_Apic_2 | 78 | 84 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 119 | 128 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 161 | 168 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 247 | 255 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.457 |
LIG_Pex14_1 | 258 | 262 | PF04695 | 0.513 |
LIG_RPA_C_Fungi | 274 | 286 | PF08784 | 0.525 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.307 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.709 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.782 |
LIG_SUMO_SIM_anti_2 | 19 | 26 | PF11976 | 0.351 |
LIG_SUMO_SIM_par_1 | 19 | 26 | PF11976 | 0.351 |
LIG_SUMO_SIM_par_1 | 288 | 293 | PF11976 | 0.572 |
LIG_TRAF2_1 | 265 | 268 | PF00917 | 0.543 |
LIG_TRAF2_1 | 55 | 58 | PF00917 | 0.307 |
LIG_TYR_ITIM | 51 | 56 | PF00017 | 0.419 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.686 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.590 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.629 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.682 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.721 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.491 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.633 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.472 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.685 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.636 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.371 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.307 |
MOD_Cter_Amidation | 10 | 13 | PF01082 | 0.690 |
MOD_Cter_Amidation | 421 | 424 | PF01082 | 0.740 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.653 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.637 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.465 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.670 |
MOD_GlcNHglycan | 198 | 203 | PF01048 | 0.682 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.686 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.708 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.557 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.744 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.742 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.622 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.475 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.657 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.646 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.562 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.779 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.685 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.714 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.424 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.301 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.484 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.614 |
MOD_N-GLC_2 | 343 | 345 | PF02516 | 0.753 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.657 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.691 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.593 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.301 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.576 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.600 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.610 |
MOD_OFUCOSY | 317 | 324 | PF10250 | 0.720 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.495 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.596 |
MOD_PKA_1 | 418 | 424 | PF00069 | 0.738 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.596 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.469 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.349 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.695 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.678 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.694 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.633 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.425 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.326 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.611 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.642 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.659 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.449 |
MOD_Plk_2-3 | 194 | 200 | PF00069 | 0.620 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.391 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.514 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.581 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.745 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.432 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.565 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.576 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.721 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.378 |
MOD_SUMO_rev_2 | 17 | 23 | PF00179 | 0.428 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.313 |
TRG_DiLeu_BaEn_1 | 20 | 25 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.368 |
TRG_DiLeu_BaEn_2 | 181 | 187 | PF01217 | 0.611 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.419 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.560 |
TRG_NES_CRM1_1 | 210 | 223 | PF08389 | 0.456 |
TRG_NLS_Bipartite_1 | 407 | 427 | PF00514 | 0.659 |
TRG_NLS_MonoExtC_3 | 8 | 13 | PF00514 | 0.703 |
TRG_NLS_MonoExtN_4 | 405 | 411 | PF00514 | 0.686 |
TRG_NLS_MonoExtN_4 | 9 | 16 | PF00514 | 0.584 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBI5 | Leptomonas seymouri | 50% | 100% |
A0A1X0NVH3 | Trypanosomatidae | 33% | 100% |
A0A3S7WY90 | Leishmania donovani | 86% | 100% |
A0A422N8J6 | Trypanosoma rangeli | 32% | 100% |
A4HDF7 | Leishmania braziliensis | 74% | 100% |
A4I0T8 | Leishmania infantum | 85% | 100% |
D0A770 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4QAN2 | Leishmania major | 86% | 100% |