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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005689 | U12-type spliceosomal complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HIL1
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.566 |
CLV_MEL_PAP_1 | 227 | 233 | PF00089 | 0.551 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.657 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.374 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.368 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.748 |
DOC_CKS1_1 | 388 | 393 | PF01111 | 0.513 |
DOC_CKS1_1 | 460 | 465 | PF01111 | 0.532 |
DOC_MAPK_MEF2A_6 | 75 | 82 | PF00069 | 0.371 |
DOC_MAPK_NFAT4_5 | 75 | 83 | PF00069 | 0.373 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.524 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.544 |
DOC_PP4_FxxP_1 | 384 | 387 | PF00568 | 0.483 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.729 |
LIG_14-3-3_CanoR_1 | 176 | 184 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 190 | 198 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 226 | 230 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 307 | 311 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 354 | 359 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 360 | 365 | PF00244 | 0.503 |
LIG_APCC_ABBA_1 | 209 | 214 | PF00400 | 0.747 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.773 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.655 |
LIG_BRCT_BRCA1_1 | 53 | 57 | PF00533 | 0.372 |
LIG_Clathr_ClatBox_1 | 85 | 89 | PF01394 | 0.413 |
LIG_CtBP_PxDLS_1 | 418 | 422 | PF00389 | 0.529 |
LIG_DLG_GKlike_1 | 354 | 362 | PF00625 | 0.531 |
LIG_EVH1_1 | 384 | 388 | PF00568 | 0.485 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.775 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.697 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.630 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.726 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.412 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.438 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.533 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.615 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.501 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.851 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.614 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.541 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.578 |
LIG_LIR_Apic_2 | 102 | 108 | PF02991 | 0.673 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.403 |
LIG_LIR_Apic_2 | 93 | 99 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 378 | 388 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 378 | 383 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.466 |
LIG_MYND_1 | 161 | 165 | PF01753 | 0.719 |
LIG_MYND_1 | 463 | 467 | PF01753 | 0.515 |
LIG_PDZ_Class_2 | 463 | 468 | PF00595 | 0.522 |
LIG_Pex14_1 | 380 | 384 | PF04695 | 0.499 |
LIG_SH2_PTP2 | 382 | 385 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.502 |
LIG_SH3_1 | 382 | 388 | PF00018 | 0.490 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.783 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.700 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.681 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.754 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.490 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.558 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.527 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.526 |
LIG_SUMO_SIM_par_1 | 279 | 285 | PF11976 | 0.468 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.755 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.638 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.568 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.505 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.847 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.605 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.530 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.577 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.548 |
MOD_Cter_Amidation | 248 | 251 | PF01082 | 0.550 |
MOD_DYRK1A_RPxSP_1 | 255 | 259 | PF00069 | 0.719 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.626 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.532 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.524 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.527 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.496 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.380 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.615 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.705 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.666 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.796 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.690 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.625 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.820 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.411 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.396 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.539 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.488 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.534 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.533 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.467 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.471 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.669 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.593 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.364 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.536 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.537 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.655 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.411 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.603 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.435 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.536 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.499 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.455 |
MOD_NEK2_2 | 225 | 230 | PF00069 | 0.542 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.686 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.721 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.677 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.541 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.513 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.531 |
MOD_PKB_1 | 407 | 415 | PF00069 | 0.577 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.534 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.499 |
MOD_Plk_2-3 | 400 | 406 | PF00069 | 0.577 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.558 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.521 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.523 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.545 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.591 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.716 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.530 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.508 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.552 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.529 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.725 |
TRG_DiLeu_BaEn_2 | 207 | 213 | PF01217 | 0.483 |
TRG_DiLeu_BaEn_2 | 284 | 290 | PF01217 | 0.712 |
TRG_DiLeu_BaLyEn_6 | 461 | 466 | PF01217 | 0.559 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.662 |
TRG_NES_CRM1_1 | 77 | 91 | PF08389 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 334 | 338 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD74 | Leptomonas seymouri | 30% | 100% |
A0A3S7X3N7 | Leishmania donovani | 67% | 100% |
A4I5V6 | Leishmania infantum | 67% | 100% |
E9B151 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4Q715 | Leishmania major | 67% | 100% |