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: Q4QGD1
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:0006996 | organelle organization | 4 | 2 |
GO:0007129 | homologous chromosome pairing at meiosis | 4 | 2 |
GO:0007131 | reciprocal meiotic recombination | 3 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016925 | protein sumoylation | 7 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018205 | peptidyl-lysine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 6 |
GO:0022414 | reproductive process | 1 | 6 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0035825 | homologous recombination | 6 | 6 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 2 |
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:0051276 | chromosome organization | 5 | 2 |
GO:0070192 | chromosome organization involved in meiotic cell cycle | 3 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
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:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1903046 | meiotic cell cycle process | 2 | 6 |
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 | 0.414 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.395 |
DEG_APCC_DBOX_1 | 90 | 98 | PF00400 | 0.399 |
DEG_SPOP_SBC_1 | 399 | 403 | PF00917 | 0.512 |
DOC_CKS1_1 | 372 | 377 | PF01111 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 372 | 378 | PF00134 | 0.549 |
DOC_PP4_FxxP_1 | 410 | 413 | PF00568 | 0.575 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.526 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 150 | 159 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 175 | 183 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 222 | 228 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 234 | 243 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 294 | 303 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 312 | 316 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 333 | 339 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 400 | 406 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 408 | 413 | PF00244 | 0.568 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.386 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.583 |
LIG_BRCT_BRCA1_1 | 366 | 370 | PF00533 | 0.480 |
LIG_Clathr_ClatBox_1 | 50 | 54 | PF01394 | 0.383 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.550 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.549 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.381 |
LIG_LIR_Apic_2 | 231 | 235 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.377 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.619 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.304 |
LIG_SH3_1 | 209 | 215 | PF00018 | 0.567 |
LIG_SH3_2 | 301 | 306 | PF14604 | 0.560 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.799 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.567 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.558 |
LIG_SUMO_SIM_par_1 | 49 | 54 | PF11976 | 0.332 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.369 |
MOD_CDK_SPK_2 | 224 | 229 | PF00069 | 0.562 |
MOD_CDK_SPK_2 | 328 | 333 | PF00069 | 0.568 |
MOD_CDK_SPK_2 | 409 | 414 | PF00069 | 0.573 |
MOD_CDK_SPxxK_3 | 336 | 343 | PF00069 | 0.558 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.572 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.561 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.588 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.578 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.519 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.538 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.508 |
MOD_GlcNHglycan | 270 | 274 | PF01048 | 0.705 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.708 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.588 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.520 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.373 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.511 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.580 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.565 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.307 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.572 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.537 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.556 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.547 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.406 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.331 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.436 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.523 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.398 |
MOD_PKA_1 | 150 | 156 | PF00069 | 0.481 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.396 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.466 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.548 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.571 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.573 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.556 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.559 |
MOD_PKB_1 | 294 | 302 | PF00069 | 0.584 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.566 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.572 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.543 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.441 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.551 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.570 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.558 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.579 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.571 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.552 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.516 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.568 |
TRG_DiLeu_BaEn_4 | 127 | 133 | PF01217 | 0.371 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.635 |
TRG_ER_diArg_1 | 304 | 307 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.571 |
TRG_NLS_MonoExtC_3 | 292 | 298 | PF00514 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WSB0 | Leishmania donovani | 93% | 100% |
A4HHR7 | Leishmania braziliensis | 64% | 83% |
A4HVF8 | Leishmania infantum | 94% | 100% |
E9AP57 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |