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: 3 |
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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 15 |
GO:0032991 | protein-containing complex | 1 | 15 |
GO:0043226 | organelle | 2 | 15 |
GO:0043228 | non-membrane-bounded organelle | 3 | 15 |
GO:0043229 | intracellular organelle | 3 | 15 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:1990904 | ribonucleoprotein complex | 2 | 15 |
Related structures:
AlphaFold database: A4ICS7
Term | Name | Level | Count |
---|---|---|---|
GO:0007165 | signal transduction | 2 | 2 |
GO:0009987 | cellular process | 1 | 4 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016310 | phosphorylation | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016301 | kinase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 467 | 471 | PF00656 | 0.345 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 388 | 390 | PF00082 | 0.741 |
CLV_PCSK_PC1ET2_1 | 419 | 421 | PF00082 | 0.295 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.403 |
DEG_APCC_DBOX_1 | 406 | 414 | PF00400 | 0.317 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.540 |
DEG_SCF_FBW7_1 | 67 | 74 | PF00400 | 0.540 |
DEG_SPOP_SBC_1 | 210 | 214 | PF00917 | 0.525 |
DOC_CYCLIN_yCln2_LP_2 | 93 | 99 | PF00134 | 0.495 |
DOC_MAPK_gen_1 | 322 | 331 | PF00069 | 0.363 |
DOC_PP1_RVXF_1 | 154 | 161 | PF00149 | 0.534 |
DOC_PP1_RVXF_1 | 474 | 480 | PF00149 | 0.482 |
DOC_PP2B_LxvP_1 | 93 | 96 | PF13499 | 0.460 |
DOC_PP4_FxxP_1 | 314 | 317 | PF00568 | 0.378 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.565 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 106 | 110 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 137 | 143 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 175 | 184 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 230 | 236 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 243 | 251 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 261 | 266 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 322 | 331 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 389 | 393 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 432 | 438 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 463 | 473 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 49 | 59 | PF00244 | 0.694 |
LIG_BRCT_BRCA1_1 | 116 | 120 | PF00533 | 0.685 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.528 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.476 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.407 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.361 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.689 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.434 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.482 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.534 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.399 |
LIG_LIR_Apic_2 | 312 | 317 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.477 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.347 |
LIG_SH3_5 | 28 | 32 | PF00018 | 0.541 |
LIG_Sin3_3 | 155 | 162 | PF02671 | 0.270 |
LIG_Sin3_3 | 408 | 415 | PF02671 | 0.306 |
LIG_SUMO_SIM_anti_2 | 356 | 361 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 326 | 332 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 455 | 461 | PF11976 | 0.368 |
LIG_TRAF2_1 | 343 | 346 | PF00917 | 0.316 |
LIG_TRFH_1 | 142 | 146 | PF08558 | 0.317 |
LIG_UBA3_1 | 220 | 228 | PF00899 | 0.515 |
MOD_CDC14_SPxK_1 | 372 | 375 | PF00782 | 0.466 |
MOD_CDK_SPxK_1 | 369 | 375 | PF00069 | 0.452 |
MOD_CDK_SPxxK_3 | 369 | 376 | PF00069 | 0.485 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.506 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.648 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.580 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.359 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.454 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.534 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.565 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.442 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.373 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.659 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.578 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.525 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.393 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.531 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.654 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.629 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.681 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.301 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.446 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.423 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.457 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.657 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.593 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.411 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.619 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.617 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.720 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.504 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.429 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.594 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.420 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.329 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.513 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.421 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.737 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.487 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.393 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.642 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.605 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.582 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.442 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.428 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.493 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.382 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.412 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.390 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.437 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.457 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.445 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.452 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.620 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.517 |
MOD_OFUCOSY | 127 | 133 | PF10250 | 0.492 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.530 |
MOD_PKA_1 | 388 | 394 | PF00069 | 0.507 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.476 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.676 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.624 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.393 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.525 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.507 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.502 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.493 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.454 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.442 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.540 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.534 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.653 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.508 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.530 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.423 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.676 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.506 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.404 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.478 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.358 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.703 |
TRG_DiLeu_BaEn_1 | 187 | 192 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_1 | 345 | 350 | PF01217 | 0.315 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.640 |
TRG_NLS_Bipartite_1 | 419 | 435 | PF00514 | 0.374 |
TRG_NLS_MonoExtC_3 | 430 | 436 | PF00514 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 486 | 490 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 57 | 61 | PF00026 | 0.632 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I384 | Leptomonas seymouri | 26% | 69% |
A0A0N1ILR3 | Leptomonas seymouri | 51% | 88% |
A0A0S4J2H1 | Bodo saltans | 30% | 100% |
A0A1X0NT03 | Trypanosomatidae | 26% | 88% |
A0A3Q8IDW5 | Leishmania donovani | 27% | 70% |
A0A3Q8IGX5 | Leishmania donovani | 99% | 100% |
A0A3R7NBP1 | Trypanosoma rangeli | 26% | 91% |
A4H8W6 | Leishmania braziliensis | 25% | 70% |
A4HX90 | Leishmania infantum | 27% | 80% |
C9ZTV9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 90% |
E9AQZ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 70% |
E9ASH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QEH1 | Leishmania major | 27% | 74% |