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: A4HHR7
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_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 436 | 440 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.421 |
CLV_PCSK_FUR_1 | 23 | 27 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.714 |
CLV_PCSK_PC7_1 | 229 | 235 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.621 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.597 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.477 |
DEG_SPOP_SBC_1 | 394 | 398 | PF00917 | 0.534 |
DOC_CKS1_1 | 449 | 454 | PF01111 | 0.704 |
DOC_CYCLIN_yCln2_LP_2 | 449 | 455 | PF00134 | 0.705 |
DOC_MAPK_gen_1 | 86 | 94 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 383 | 391 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 61 | 69 | PF00069 | 0.447 |
DOC_PP1_RVXF_1 | 442 | 448 | PF00149 | 0.573 |
DOC_PP4_FxxP_1 | 494 | 497 | PF00568 | 0.717 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.482 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 234 | 243 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 448 | 452 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 492 | 497 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 61 | 66 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 91 | 95 | PF00244 | 0.404 |
LIG_Actin_WH2_2 | 468 | 486 | PF00022 | 0.544 |
LIG_Clathr_ClatBox_1 | 141 | 145 | PF01394 | 0.531 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.327 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.523 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.723 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.551 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.548 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.705 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.467 |
LIG_LIR_Nem_3 | 93 | 97 | PF02991 | 0.522 |
LIG_MYND_1 | 242 | 246 | PF01753 | 0.545 |
LIG_MYND_1 | 485 | 489 | PF01753 | 0.527 |
LIG_PDZ_Class_2 | 499 | 504 | PF00595 | 0.511 |
LIG_SH2_CRK | 139 | 143 | PF00017 | 0.629 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.454 |
LIG_SH3_1 | 294 | 300 | PF00018 | 0.717 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.793 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.721 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.595 |
LIG_TRAF2_1 | 53 | 56 | PF00917 | 0.524 |
LIG_TRFH_1 | 481 | 485 | PF08558 | 0.531 |
LIG_WRC_WIRS_1 | 471 | 476 | PF05994 | 0.561 |
LIG_WW_2 | 242 | 245 | PF00397 | 0.524 |
MOD_CDK_SPK_2 | 404 | 409 | PF00069 | 0.687 |
MOD_CDK_SPK_2 | 493 | 498 | PF00069 | 0.716 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.463 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.696 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.640 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.568 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.580 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.450 |
MOD_Cter_Amidation | 72 | 75 | PF01082 | 0.456 |
MOD_Cter_Amidation | 84 | 87 | PF01082 | 0.418 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.533 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.544 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.578 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.656 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.601 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.655 |
MOD_GlcNHglycan | 7 | 11 | PF01048 | 0.484 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.539 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.699 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.602 |
MOD_LATS_1 | 490 | 496 | PF00433 | 0.551 |
MOD_N-GLC_2 | 19 | 21 | PF02516 | 0.460 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.718 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.709 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.553 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.414 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.605 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.483 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.551 |
MOD_PK_1 | 61 | 67 | PF00069 | 0.447 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.335 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.497 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.783 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.733 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.540 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.698 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.392 |
MOD_PKB_1 | 370 | 378 | PF00069 | 0.721 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.787 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.699 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.608 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.471 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.566 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.715 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.664 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.713 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.680 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.714 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.623 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.589 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 74 | 76 | PF00400 | 0.461 |
TRG_NLS_MonoExtC_3 | 368 | 374 | PF00514 | 0.717 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WSB0 | Leishmania donovani | 65% | 100% |
A4HVF8 | Leishmania infantum | 65% | 100% |
E9AP57 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
Q4QGD1 | Leishmania major | 64% | 98% |