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: E9AP57
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:0005488 | binding | 1 | 4 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 6 |
GO:0019789 | SUMO transferase activity | 4 | 6 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043169 | cation binding | 3 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.753 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.757 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.599 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.812 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.812 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.662 |
DEG_APCC_DBOX_1 | 90 | 98 | PF00400 | 0.667 |
DEG_SPOP_SBC_1 | 271 | 275 | PF00917 | 0.545 |
DOC_CKS1_1 | 372 | 377 | PF01111 | 0.820 |
DOC_CYCLIN_yCln2_LP_2 | 372 | 378 | PF00134 | 0.822 |
DOC_MAPK_gen_1 | 293 | 303 | PF00069 | 0.532 |
DOC_MAPK_HePTP_8 | 206 | 218 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 209 | 218 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 365 | 371 | PF00149 | 0.603 |
DOC_PP2B_LxvP_1 | 301 | 304 | PF13499 | 0.538 |
DOC_PP4_FxxP_1 | 411 | 414 | PF00568 | 0.819 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.807 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.646 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.826 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.824 |
LIG_14-3-3_CanoR_1 | 145 | 153 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 175 | 183 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 312 | 316 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 409 | 414 | PF00244 | 0.789 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.611 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.776 |
LIG_Clathr_ClatBox_1 | 50 | 54 | PF01394 | 0.661 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.820 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.821 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.514 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.463 |
LIG_LIR_Apic_2 | 231 | 235 | PF02991 | 0.757 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.485 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.637 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.640 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.570 |
LIG_SH3_1 | 209 | 215 | PF00018 | 0.821 |
LIG_SH3_2 | 159 | 164 | PF14604 | 0.538 |
LIG_SH3_2 | 381 | 386 | PF14604 | 0.537 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.822 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.821 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.337 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.573 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.566 |
MOD_CDC14_SPxK_1 | 161 | 164 | PF00782 | 0.537 |
MOD_CDK_SPK_2 | 224 | 229 | PF00069 | 0.741 |
MOD_CDK_SPK_2 | 410 | 415 | PF00069 | 0.824 |
MOD_CDK_SPxK_1 | 158 | 164 | PF00069 | 0.537 |
MOD_CDK_SPxxK_3 | 336 | 343 | PF00069 | 0.661 |
MOD_CDK_SPxxK_3 | 360 | 367 | PF00069 | 0.528 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.401 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.687 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.563 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.773 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.595 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.615 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.504 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.469 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.632 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.798 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.628 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.529 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.516 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.519 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.810 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.653 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.594 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.534 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.626 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.807 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.708 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.471 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.706 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.530 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.629 |
MOD_LATS_1 | 251 | 257 | PF00433 | 0.677 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.809 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.530 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.821 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.640 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.413 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.710 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.698 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.560 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.534 |
MOD_PK_1 | 16 | 22 | PF00069 | 0.420 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.597 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.809 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.756 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.745 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.819 |
MOD_PKB_1 | 294 | 302 | PF00069 | 0.824 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.537 |
MOD_Plk_2-3 | 64 | 70 | PF00069 | 0.391 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.810 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.544 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.535 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.590 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.819 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.771 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.680 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.828 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.723 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.772 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.670 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.820 |
TRG_DiLeu_BaEn_4 | 127 | 133 | PF01217 | 0.567 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.631 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.642 |
TRG_ER_diArg_1 | 304 | 307 | PF00400 | 0.754 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.770 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.554 |
TRG_NLS_MonoExtC_3 | 292 | 298 | PF00514 | 0.814 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WSB0 | Leishmania donovani | 86% | 100% |
A4HHR7 | Leishmania braziliensis | 64% | 100% |
A4HVF8 | Leishmania infantum | 87% | 100% |
Q4QGD1 | Leishmania major | 85% | 100% |