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: E9ASH7
Term | Name | Level | Count |
---|---|---|---|
GO:0007165 | signal transduction | 2 | 1 |
GO:0009987 | cellular process | 1 | 3 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
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 | 0.329 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.526 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 388 | 390 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.404 |
DEG_APCC_DBOX_1 | 118 | 126 | PF00400 | 0.450 |
DEG_APCC_DBOX_1 | 406 | 414 | PF00400 | 0.330 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.540 |
DEG_SCF_FBW7_1 | 68 | 75 | PF00400 | 0.541 |
DEG_SCF_TRCP1_1 | 470 | 475 | PF00400 | 0.289 |
DEG_SPOP_SBC_1 | 210 | 214 | PF00917 | 0.412 |
DOC_CKS1_1 | 129 | 134 | PF01111 | 0.430 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 94 | 100 | PF00134 | 0.516 |
DOC_PP1_RVXF_1 | 154 | 161 | PF00149 | 0.304 |
DOC_PP1_RVXF_1 | 386 | 393 | PF00149 | 0.577 |
DOC_PP1_RVXF_1 | 474 | 480 | PF00149 | 0.475 |
DOC_PP4_FxxP_1 | 314 | 317 | PF00568 | 0.384 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.624 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 137 | 143 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 175 | 184 | PF00244 | 0.572 |
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 | 0.459 |
LIG_14-3-3_CanoR_1 | 389 | 393 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 432 | 438 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 463 | 467 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.703 |
LIG_Actin_WH2_2 | 450 | 465 | PF00022 | 0.322 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.679 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.353 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.410 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.399 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.527 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.465 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.300 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.480 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.486 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.503 |
LIG_LIR_Apic_2 | 312 | 317 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 60 | 68 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 89 | 98 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.526 |
LIG_PTB_Apo_2 | 55 | 62 | PF02174 | 0.434 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.443 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.480 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.645 |
LIG_SH3_5 | 30 | 34 | PF00018 | 0.563 |
LIG_Sin3_3 | 408 | 415 | PF02671 | 0.314 |
LIG_SUMO_SIM_par_1 | 326 | 332 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 455 | 461 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 487 | 492 | PF11976 | 0.312 |
LIG_TRAF2_1 | 343 | 346 | PF00917 | 0.325 |
LIG_TRFH_1 | 142 | 146 | PF08558 | 0.383 |
LIG_UBA3_1 | 220 | 228 | PF00899 | 0.383 |
MOD_CDC14_SPxK_1 | 473 | 476 | PF00782 | 0.302 |
MOD_CDK_SPxK_1 | 470 | 476 | PF00069 | 0.290 |
MOD_CDK_SPxxK_3 | 128 | 135 | PF00069 | 0.429 |
MOD_CDK_SPxxK_3 | 369 | 376 | PF00069 | 0.431 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.730 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.362 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.454 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.501 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.428 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.351 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.664 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.583 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.525 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.405 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.735 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.309 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.552 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.437 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.488 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.471 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.685 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.382 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.592 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.617 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.619 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.621 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.388 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.570 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.412 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.425 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.340 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.439 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.545 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.743 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.501 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.380 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.647 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.604 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.485 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.434 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.447 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.336 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.468 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.495 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.393 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.411 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.409 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.433 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.445 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.445 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.627 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.510 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.515 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.537 |
MOD_PKA_1 | 388 | 394 | PF00069 | 0.471 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.701 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.617 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.393 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.525 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.471 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.527 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.353 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.407 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.321 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.444 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.515 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.501 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.658 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.534 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.462 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.452 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.739 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.631 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.333 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.706 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.636 |
TRG_DiLeu_BaEn_1 | 187 | 192 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_1 | 345 | 350 | PF01217 | 0.319 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.594 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 486 | 490 | PF00026 | 0.306 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I384 | Leptomonas seymouri | 24% | 69% |
A0A0N1ILR3 | Leptomonas seymouri | 48% | 88% |
A0A0S4J2H1 | Bodo saltans | 30% | 100% |
A0A1X0NT03 | Trypanosomatidae | 24% | 88% |
A0A3Q8IDW5 | Leishmania donovani | 25% | 70% |
A0A3Q8IGX5 | Leishmania donovani | 85% | 100% |
A0A3R7NBP1 | Trypanosoma rangeli | 24% | 91% |
A4H8W6 | Leishmania braziliensis | 23% | 70% |
A4HX90 | Leishmania infantum | 25% | 80% |
A4ICS7 | Leishmania infantum | 85% | 100% |
C9ZTV9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 90% |
E9AQZ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 70% |
Q4QEH1 | Leishmania major | 24% | 74% |