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:0000795 | synaptonemal complex | 3 | 6 |
GO:0099086 | synaptonemal structure | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4HVF8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006259 | DNA metabolic process | 4 | 6 |
GO:0006310 | DNA recombination | 5 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0007131 | reciprocal meiotic recombination | 3 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0022402 | cell cycle process | 2 | 6 |
GO:0022414 | reproductive process | 1 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0035825 | homologous recombination | 6 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:0140527 | reciprocal homologous recombination | 7 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:1903046 | meiotic cell cycle process | 2 | 6 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007129 | homologous chromosome pairing at meiosis | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016925 | protein sumoylation | 7 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0070192 | chromosome organization involved in meiotic cell cycle | 3 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 6 |
GO:0019789 | SUMO transferase activity | 4 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:0005488 | binding | 1 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.760 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.749 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.590 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.818 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.818 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.749 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.660 |
DEG_APCC_DBOX_1 | 90 | 98 | PF00400 | 0.663 |
DOC_CKS1_1 | 371 | 376 | PF01111 | 0.791 |
DOC_CYCLIN_yCln2_LP_2 | 371 | 377 | PF00134 | 0.788 |
DOC_PP4_FxxP_1 | 409 | 412 | PF00568 | 0.817 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.807 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.738 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.828 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.817 |
LIG_14-3-3_CanoR_1 | 150 | 159 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 174 | 182 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 293 | 302 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 311 | 315 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 407 | 412 | PF00244 | 0.783 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
LIG_BRCT_BRCA1_1 | 347 | 351 | PF00533 | 0.769 |
LIG_BRCT_BRCA1_1 | 365 | 369 | PF00533 | 0.476 |
LIG_Clathr_ClatBox_1 | 50 | 54 | PF01394 | 0.650 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.810 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.791 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.602 |
LIG_LIR_Apic_2 | 230 | 234 | PF02991 | 0.763 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.480 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.631 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.595 |
LIG_SH3_1 | 208 | 214 | PF00018 | 0.828 |
LIG_SH3_2 | 300 | 305 | PF14604 | 0.716 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.810 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.828 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.714 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.615 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.563 |
MOD_CDK_SPK_2 | 223 | 228 | PF00069 | 0.760 |
MOD_CDK_SPK_2 | 327 | 332 | PF00069 | 0.790 |
MOD_CDK_SPK_2 | 408 | 413 | PF00069 | 0.817 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.389 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.799 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.690 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.556 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.772 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.608 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.617 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.585 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.800 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.636 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.810 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.651 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.574 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.824 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.714 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.470 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.714 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.718 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.588 |
MOD_LATS_1 | 250 | 256 | PF00433 | 0.667 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.816 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.793 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.639 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.409 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.694 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.674 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.507 |
MOD_PK_1 | 16 | 22 | PF00069 | 0.419 |
MOD_PKA_1 | 150 | 156 | PF00069 | 0.699 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.597 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.668 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.837 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.798 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.766 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.750 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.801 |
MOD_PKB_1 | 293 | 301 | PF00069 | 0.825 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.823 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.779 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.674 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.533 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.792 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.787 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.684 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.829 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.778 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.640 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.814 |
TRG_DiLeu_BaEn_4 | 127 | 133 | PF01217 | 0.565 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.635 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.760 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.749 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.548 |
TRG_NLS_MonoExtC_3 | 291 | 297 | PF00514 | 0.820 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WSB0 | Leishmania donovani | 100% | 100% |
A4HHR7 | Leishmania braziliensis | 65% | 100% |
E9AP57 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QGD1 | Leishmania major | 94% | 100% |