Nuclear proteins, nucleoporin (NUP54/57)
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:0005643 | nuclear pore | 3 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
GO:0044613 | nuclear pore central transport channel | 3 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I794
Term | Name | Level | Count |
---|---|---|---|
GO:0006606 | protein import into nucleus | 5 | 1 |
GO:0006607 | NLS-bearing protein import into nucleus | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0006997 | nucleus organization | 5 | 1 |
GO:0006999 | nuclear pore organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0034504 | protein localization to nucleus | 6 | 1 |
GO:0036228 | protein localization to nuclear inner membrane | 5 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051170 | import into nucleus | 6 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090435 | protein localization to nuclear envelope | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 1 |
GO:0017056 | structural constituent of nuclear pore | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.492 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.271 |
CLV_Separin_Metazoa | 253 | 257 | PF03568 | 0.278 |
CLV_Separin_Metazoa | 315 | 319 | PF03568 | 0.326 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.627 |
DOC_MAPK_DCC_7 | 242 | 250 | PF00069 | 0.240 |
DOC_MAPK_gen_1 | 256 | 267 | PF00069 | 0.324 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.250 |
DOC_PP4_FxxP_1 | 119 | 122 | PF00568 | 0.590 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.588 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.578 |
DOC_USP7_UBL2_3 | 266 | 270 | PF12436 | 0.278 |
DOC_USP7_UBL2_3 | 435 | 439 | PF12436 | 0.438 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.241 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.584 |
LIG_14-3-3_CanoR_1 | 170 | 178 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 306 | 311 | PF00244 | 0.255 |
LIG_14-3-3_CanoR_1 | 319 | 329 | PF00244 | 0.263 |
LIG_14-3-3_CanoR_1 | 346 | 354 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 355 | 365 | PF00244 | 0.365 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.462 |
LIG_Clathr_ClatBox_1 | 178 | 182 | PF01394 | 0.365 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.559 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.494 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.592 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.278 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.572 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.400 |
LIG_LIR_Apic_2 | 116 | 122 | PF02991 | 0.592 |
LIG_LIR_Apic_2 | 57 | 62 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 182 | 190 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.411 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.326 |
LIG_NRBOX | 429 | 435 | PF00104 | 0.371 |
LIG_PCNA_PIPBox_1 | 171 | 180 | PF02747 | 0.376 |
LIG_PCNA_yPIPBox_3 | 170 | 178 | PF02747 | 0.464 |
LIG_PCNA_yPIPBox_3 | 262 | 276 | PF02747 | 0.278 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.592 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.365 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.250 |
LIG_SH2_GRB2like | 219 | 222 | PF00017 | 0.490 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.491 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.631 |
LIG_SUMO_SIM_anti_2 | 363 | 369 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 161 | 167 | PF11976 | 0.579 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.537 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.525 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.581 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.326 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.234 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.404 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.330 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.624 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.532 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.514 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.538 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.557 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.558 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.553 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.540 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.505 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.497 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.450 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.507 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.498 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.555 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.356 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.372 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.382 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.553 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.595 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.531 |
MOD_N-GLC_2 | 200 | 202 | PF02516 | 0.335 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.576 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.423 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.499 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.591 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.326 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.537 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.549 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.356 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.316 |
MOD_PIKK_1 | 366 | 372 | PF00454 | 0.470 |
MOD_PKA_1 | 270 | 276 | PF00069 | 0.290 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.482 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.475 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.326 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.302 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.424 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.504 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.442 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.250 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.241 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.585 |
MOD_SUMO_rev_2 | 432 | 441 | PF00179 | 0.441 |
TRG_DiLeu_BaEn_2 | 352 | 358 | PF01217 | 0.250 |
TRG_DiLeu_BaLyEn_6 | 399 | 404 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.250 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 290 | 292 | PF00400 | 0.367 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICT1 | Leishmania donovani | 99% | 100% |
A0A3R7KYW1 | Trypanosoma rangeli | 41% | 100% |
A4HJS8 | Leishmania braziliensis | 79% | 100% |
E9B289 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4Q5W9 | Leishmania major | 94% | 100% |