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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0070390 | transcription export complex 2 | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4ICH0
Term | Name | Level | Count |
---|---|---|---|
GO:0006405 | RNA export from nucleus | 5 | 12 |
GO:0006406 | mRNA export from nucleus | 6 | 12 |
GO:0006810 | transport | 3 | 12 |
GO:0006913 | nucleocytoplasmic transport | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015931 | nucleobase-containing compound transport | 5 | 12 |
GO:0016973 | poly(A)+ mRNA export from nucleus | 7 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0050657 | nucleic acid transport | 6 | 12 |
GO:0050658 | RNA transport | 4 | 12 |
GO:0051028 | mRNA transport | 5 | 12 |
GO:0051168 | nuclear export | 6 | 12 |
GO:0051169 | nuclear transport | 4 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051236 | establishment of RNA localization | 3 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0000972 | transcription-dependent tethering of RNA polymerase II gene DNA at nuclear periphery | 6 | 1 |
GO:0000973 | post-transcriptional tethering of RNA polymerase II gene DNA at nuclear periphery | 7 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006354 | DNA-templated transcription elongation | 6 | 1 |
GO:0006368 | transcription elongation by RNA polymerase II | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 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 | 451 | 455 | PF00656 | 0.456 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.401 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 486 | 488 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.470 |
CLV_Separin_Metazoa | 380 | 384 | PF03568 | 0.438 |
DEG_APCC_DBOX_1 | 235 | 243 | PF00400 | 0.341 |
DEG_APCC_DBOX_1 | 256 | 264 | PF00400 | 0.401 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.543 |
DEG_SCF_FBW7_2 | 85 | 90 | PF00400 | 0.491 |
DOC_CYCLIN_RxL_1 | 163 | 173 | PF00134 | 0.376 |
DOC_CYCLIN_yCln2_LP_2 | 344 | 347 | PF00134 | 0.344 |
DOC_MAPK_gen_1 | 233 | 242 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 255 | 262 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 34 | 43 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 356 | 364 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 421 | 428 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 101 | 109 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 233 | 242 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 34 | 43 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 421 | 428 | PF00069 | 0.471 |
DOC_PP1_RVXF_1 | 359 | 365 | PF00149 | 0.329 |
DOC_PP2B_LxvP_1 | 344 | 347 | PF13499 | 0.369 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.382 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.583 |
LIG_14-3-3_CanoR_1 | 158 | 168 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 273 | 282 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 308 | 317 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 363 | 369 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 526 | 536 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.501 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.521 |
LIG_EVH1_2 | 346 | 350 | PF00568 | 0.536 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.336 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.475 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.307 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.535 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.408 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.595 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.571 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.353 |
LIG_GBD_Chelix_1 | 262 | 270 | PF00786 | 0.385 |
LIG_HCF-1_HBM_1 | 2 | 5 | PF13415 | 0.455 |
LIG_Integrin_isoDGR_2 | 373 | 375 | PF01839 | 0.475 |
LIG_Integrin_RGD_1 | 402 | 404 | PF01839 | 0.339 |
LIG_LIR_Gen_1 | 197 | 208 | PF02991 | 0.311 |
LIG_LIR_LC3C_4 | 102 | 105 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 316 | 320 | PF02991 | 0.395 |
LIG_NRBOX | 164 | 170 | PF00104 | 0.485 |
LIG_PCNA_PIPBox_1 | 430 | 439 | PF02747 | 0.351 |
LIG_PCNA_yPIPBox_3 | 430 | 442 | PF02747 | 0.355 |
LIG_PDZ_Class_3 | 546 | 551 | PF00595 | 0.518 |
LIG_RPA_C_Fungi | 437 | 449 | PF08784 | 0.437 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.362 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.350 |
LIG_SH2_STAT3 | 69 | 72 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.547 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.506 |
LIG_SUMO_SIM_anti_2 | 201 | 207 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 238 | 244 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 534 | 539 | PF11976 | 0.341 |
LIG_TRAF2_1 | 174 | 177 | PF00917 | 0.390 |
LIG_TRAF2_1 | 471 | 474 | PF00917 | 0.444 |
LIG_TRFH_1 | 342 | 346 | PF08558 | 0.334 |
LIG_TYR_ITIM | 340 | 345 | PF00017 | 0.402 |
LIG_TYR_ITIM | 434 | 439 | PF00017 | 0.381 |
LIG_WRC_WIRS_1 | 172 | 177 | PF05994 | 0.403 |
LIG_WW_3 | 186 | 190 | PF00397 | 0.564 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.672 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.421 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.374 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.507 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.530 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.789 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.579 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.398 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.545 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.522 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.347 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.405 |
MOD_Cter_Amidation | 373 | 376 | PF01082 | 0.491 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.640 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.509 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.478 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.448 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.724 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.690 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.481 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.574 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.715 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.424 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.484 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.427 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.505 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.689 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.481 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.366 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.408 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.545 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.605 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.494 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.353 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.357 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.626 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.495 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.505 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.610 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.388 |
MOD_PKA_1 | 485 | 491 | PF00069 | 0.736 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.449 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.479 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.406 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.594 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.317 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.534 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.422 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.411 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.351 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.347 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.429 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.311 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.368 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.472 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.428 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.345 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.545 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.333 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.448 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.658 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.509 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.574 |
MOD_SUMO_for_1 | 33 | 36 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 530 | 536 | PF00179 | 0.329 |
TRG_DiLeu_BaEn_1 | 532 | 537 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 542 | 547 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 375 | 377 | PF00400 | 0.499 |
TRG_NLS_MonoExtC_3 | 484 | 489 | PF00514 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 329 | 333 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTB0 | Leptomonas seymouri | 71% | 100% |
A0A0S4J9T0 | Bodo saltans | 41% | 99% |
A0A1X0NKD6 | Trypanosomatidae | 45% | 100% |
A0A3R7LU45 | Trypanosoma rangeli | 43% | 100% |
A0A3S7XAY0 | Leishmania donovani | 100% | 100% |
A4HPD0 | Leishmania braziliensis | 90% | 100% |
D0A3J0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 99% |
E9AT41 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4Q1F7 | Leishmania major | 97% | 100% |
V5BKA5 | Trypanosoma cruzi | 43% | 100% |