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 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
GO:1990904 | ribonucleoprotein complex | 2 | 7 |
GO:0005682 | U5 snRNP | 5 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 1 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 1 |
GO:0071020 | post-spliceosomal complex | 4 | 1 |
GO:0071021 | U2-type post-spliceosomal complex | 5 | 1 |
GO:0097525 | spliceosomal snRNP complex | 4 | 1 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 1 |
GO:0120114 | Sm-like protein family complex | 2 | 1 |
Related structures:
AlphaFold database: A4HCE1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006396 | RNA processing | 6 | 6 |
GO:0006397 | mRNA processing | 7 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0008380 | RNA splicing | 7 | 6 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 6 |
GO:0016071 | mRNA metabolic process | 6 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 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:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:0000350 | generation of catalytic spliceosome for second transesterification step | 7 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 299 | 303 | PF00656 | 0.655 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.271 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 109 | 111 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.624 |
DEG_APCC_DBOX_1 | 443 | 451 | PF00400 | 0.471 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.493 |
DEG_ODPH_VHL_1 | 362 | 375 | PF01847 | 0.486 |
DEG_SCF_FBW7_1 | 260 | 265 | PF00400 | 0.415 |
DEG_SPOP_SBC_1 | 125 | 129 | PF00917 | 0.528 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.553 |
DOC_CKS1_1 | 259 | 264 | PF01111 | 0.388 |
DOC_CYCLIN_yCln2_LP_2 | 324 | 330 | PF00134 | 0.249 |
DOC_MAPK_FxFP_2 | 536 | 539 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 405 | 413 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 444 | 452 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 456 | 464 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 465 | 473 | PF00069 | 0.520 |
DOC_PP2B_LxvP_1 | 361 | 364 | PF13499 | 0.417 |
DOC_PP2B_LxvP_1 | 437 | 440 | PF13499 | 0.332 |
DOC_PP4_FxxP_1 | 245 | 248 | PF00568 | 0.368 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.475 |
DOC_PP4_FxxP_1 | 536 | 539 | PF00568 | 0.423 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.545 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.523 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 143 | 149 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 491 | 495 | PF00244 | 0.471 |
LIG_APCC_ABBA_1 | 521 | 526 | PF00400 | 0.520 |
LIG_BRCT_BRCA1_1 | 241 | 245 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 533 | 537 | PF00533 | 0.496 |
LIG_CtBP_PxDLS_1 | 440 | 444 | PF00389 | 0.415 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.656 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.639 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.562 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.520 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.458 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.568 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.490 |
LIG_Integrin_isoDGR_2 | 346 | 348 | PF01839 | 0.618 |
LIG_LIR_Apic_2 | 242 | 248 | PF02991 | 0.380 |
LIG_LIR_Apic_2 | 534 | 539 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 279 | 290 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 458 | 469 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 458 | 464 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.471 |
LIG_MLH1_MIPbox_1 | 533 | 537 | PF16413 | 0.496 |
LIG_NRBOX | 330 | 336 | PF00104 | 0.312 |
LIG_NRBOX | 5 | 11 | PF00104 | 0.578 |
LIG_SH2_PTP2 | 468 | 471 | PF00017 | 0.528 |
LIG_SH2_SRC | 468 | 471 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.406 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.599 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.723 |
LIG_SH3_CIN85_PxpxPR_1 | 244 | 249 | PF14604 | 0.344 |
LIG_SUMO_SIM_par_1 | 80 | 86 | PF11976 | 0.403 |
LIG_UBA3_1 | 284 | 289 | PF00899 | 0.453 |
MOD_CDC14_SPxK_1 | 529 | 532 | PF00782 | 0.530 |
MOD_CDK_SPxK_1 | 526 | 532 | PF00069 | 0.415 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.586 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.675 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.545 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.568 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.443 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.539 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.549 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.583 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.580 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.579 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.423 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.384 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.578 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.522 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.411 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.471 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.606 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.538 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.586 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.566 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.385 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.608 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.650 |
MOD_GlcNHglycan | 25 | 30 | PF01048 | 0.655 |
MOD_GlcNHglycan | 422 | 426 | PF01048 | 0.446 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.271 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.587 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.557 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.675 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.618 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.561 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.592 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.649 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.629 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.396 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.447 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.419 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.603 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.651 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.428 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.627 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.531 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.529 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.475 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.500 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.497 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.446 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.714 |
MOD_NEK2_2 | 83 | 88 | PF00069 | 0.401 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.305 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.611 |
MOD_PIKK_1 | 362 | 368 | PF00454 | 0.385 |
MOD_PKA_1 | 267 | 273 | PF00069 | 0.478 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.537 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.578 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.471 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.432 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.501 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.467 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.501 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.423 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.520 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.446 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.534 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.420 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.387 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.452 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.572 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.544 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.528 |
MOD_SUMO_for_1 | 288 | 291 | PF00179 | 0.471 |
MOD_SUMO_rev_2 | 113 | 122 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 302 | 311 | PF00179 | 0.587 |
TRG_DiLeu_BaEn_2 | 519 | 525 | PF01217 | 0.471 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.497 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.473 |
TRG_NES_CRM1_1 | 274 | 287 | PF08389 | 0.471 |
TRG_NES_CRM1_1 | 323 | 337 | PF08389 | 0.402 |
TRG_NLS_MonoExtC_3 | 10 | 15 | PF00514 | 0.612 |
TRG_NLS_MonoExtN_4 | 11 | 16 | PF00514 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 249 | 253 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 453 | 457 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I883 | Leptomonas seymouri | 44% | 100% |
A0A3Q8ICC8 | Leishmania donovani | 74% | 99% |
A4HZW5 | Leishmania infantum | 73% | 99% |
E9AVS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 99% |
Q4QBQ6 | Leishmania major | 73% | 99% |