LeishMANIAdb
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Nucleoporin

Quick info Localization Expansion Sequence features Structure Putative motif mimicry Homologs Download

Quick info

Protein:
Nucleoporin
Gene product:
Nucleoporin NUP53b
Species:
Leishmania mexicana
UniProt:
E9ALZ8_LEIMU
TriTrypDb:
LmxM.08_29.0800
Length:
673

Localization

Secreted promastigote
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
Secreted amastigote
Source Evidence on protein Close homologs
Pires et al. no yes: 0
Exosome
Source Evidence on protein Close homologs
Silverman et al. no yes: 0
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 0
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 5
NetGPI no yes: 0, no: 5
Cellular components
Term Name Level Count
GO:0005643 nuclear pore 3 1
GO:0032991 protein-containing complex 1 1
GO:0044613 nuclear pore central transport channel 3 1
GO:0140513 nuclear protein-containing complex 2 1

Expansion

Sequence features

E9ALZ8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9ALZ8

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 221 225 PF00656 0.492
CLV_NRD_NRD_1 247 249 PF00675 0.611
CLV_NRD_NRD_1 280 282 PF00675 0.616
CLV_NRD_NRD_1 346 348 PF00675 0.593
CLV_NRD_NRD_1 453 455 PF00675 0.666
CLV_PCSK_KEX2_1 280 282 PF00082 0.604
CLV_PCSK_KEX2_1 346 348 PF00082 0.593
CLV_PCSK_KEX2_1 453 455 PF00082 0.666
CLV_PCSK_SKI1_1 18 22 PF00082 0.633
CLV_PCSK_SKI1_1 248 252 PF00082 0.611
CLV_PCSK_SKI1_1 423 427 PF00082 0.565
DEG_APCC_DBOX_1 247 255 PF00400 0.612
DEG_APCC_DBOX_1 279 287 PF00400 0.587
DEG_SPOP_SBC_1 242 246 PF00917 0.620
DEG_SPOP_SBC_1 479 483 PF00917 0.706
DOC_CDC14_PxL_1 460 468 PF14671 0.707
DOC_CYCLIN_yCln2_LP_2 362 365 PF00134 0.657
DOC_MAPK_gen_1 211 217 PF00069 0.583
DOC_PP1_RVXF_1 170 177 PF00149 0.617
DOC_PP2B_LxvP_1 362 365 PF13499 0.657
DOC_PP4_FxxP_1 461 464 PF00568 0.703
DOC_PP4_FxxP_1 530 533 PF00568 0.688
DOC_USP7_MATH_1 235 239 PF00917 0.666
DOC_USP7_MATH_1 240 244 PF00917 0.584
DOC_USP7_MATH_1 27 31 PF00917 0.740
DOC_USP7_MATH_1 327 331 PF00917 0.668
DOC_USP7_MATH_1 336 340 PF00917 0.549
DOC_USP7_MATH_1 372 376 PF00917 0.658
DOC_USP7_MATH_1 455 459 PF00917 0.675
DOC_USP7_MATH_1 607 611 PF00917 0.664
DOC_USP7_MATH_1 620 624 PF00917 0.570
DOC_USP7_MATH_1 656 660 PF00917 0.729
DOC_USP7_MATH_1 661 665 PF00917 0.690
DOC_WW_Pin1_4 25 30 PF00397 0.789
DOC_WW_Pin1_4 332 337 PF00397 0.629
DOC_WW_Pin1_4 453 458 PF00397 0.672
DOC_WW_Pin1_4 473 478 PF00397 0.578
LIG_Actin_WH2_2 306 323 PF00022 0.485
LIG_Actin_WH2_2 355 372 PF00022 0.657
LIG_Actin_WH2_2 391 408 PF00022 0.492
LIG_APCC_ABBAyCdc20_2 200 206 PF00400 0.568
LIG_BIR_II_1 1 5 PF00653 0.670
LIG_BRCT_BRCA1_1 457 461 PF00533 0.687
LIG_FHA_1 120 126 PF00498 0.684
LIG_FHA_1 178 184 PF00498 0.595
LIG_FHA_1 495 501 PF00498 0.639
LIG_FHA_1 616 622 PF00498 0.518
LIG_FHA_2 354 360 PF00498 0.609
LIG_FHA_2 457 463 PF00498 0.693
LIG_GBD_Chelix_1 340 348 PF00786 0.585
LIG_LIR_Apic_2 458 464 PF02991 0.697
LIG_LIR_Apic_2 527 533 PF02991 0.689
LIG_LIR_Gen_1 173 183 PF02991 0.733
LIG_LIR_Gen_1 335 344 PF02991 0.600
LIG_LIR_Nem_3 173 179 PF02991 0.730
LIG_LIR_Nem_3 2 6 PF02991 0.623
LIG_LIR_Nem_3 244 250 PF02991 0.616
LIG_LIR_Nem_3 335 340 PF02991 0.613
LIG_LIR_Nem_3 458 463 PF02991 0.696
LIG_LYPXL_yS_3 158 161 PF13949 0.594
LIG_MLH1_MIPbox_1 457 461 PF16413 0.687
LIG_NRP_CendR_1 671 673 PF00754 0.749
LIG_PTAP_UEV_1 621 626 PF05743 0.652
LIG_REV1ctd_RIR_1 423 432 PF16727 0.462
LIG_SH2_CRK 247 251 PF00017 0.618
LIG_SH2_GRB2like 216 219 PF00017 0.592
LIG_SH2_STAP1 296 300 PF00017 0.573
LIG_SH2_STAT5 214 217 PF00017 0.587
LIG_SH2_STAT5 460 463 PF00017 0.703
LIG_SH3_2 365 370 PF14604 0.567
LIG_SH3_3 142 148 PF00018 0.758
LIG_SH3_3 297 303 PF00018 0.579
LIG_SH3_3 362 368 PF00018 0.559
LIG_SH3_3 461 467 PF00018 0.706
LIG_SH3_3 550 556 PF00018 0.503
LIG_SH3_3 619 625 PF00018 0.702
LIG_SH3_3 626 632 PF00018 0.628
LIG_UBA3_1 250 258 PF00899 0.607
LIG_WRC_WIRS_1 199 204 PF05994 0.577
LIG_WW_2 464 467 PF00397 0.709
MOD_CK1_1 119 125 PF00069 0.763
MOD_CK1_1 177 183 PF00069 0.618
MOD_CK1_1 238 244 PF00069 0.593
MOD_CK1_1 353 359 PF00069 0.600
MOD_CK1_1 456 462 PF00069 0.690
MOD_CK1_1 623 629 PF00069 0.629
MOD_CK2_1 336 342 PF00069 0.558
MOD_CK2_1 353 359 PF00069 0.600
MOD_GlcNHglycan 114 117 PF01048 0.632
MOD_GlcNHglycan 122 125 PF01048 0.602
MOD_GlcNHglycan 224 227 PF01048 0.600
MOD_GlcNHglycan 237 240 PF01048 0.652
MOD_GlcNHglycan 315 318 PF01048 0.692
MOD_GlcNHglycan 352 355 PF01048 0.588
MOD_GlcNHglycan 374 377 PF01048 0.667
MOD_GlcNHglycan 383 386 PF01048 0.526
MOD_GlcNHglycan 41 44 PF01048 0.656
MOD_GlcNHglycan 483 486 PF01048 0.735
MOD_GlcNHglycan 497 500 PF01048 0.669
MOD_GlcNHglycan 507 510 PF01048 0.613
MOD_GlcNHglycan 574 577 PF01048 0.613
MOD_GlcNHglycan 609 612 PF01048 0.657
MOD_GlcNHglycan 622 625 PF01048 0.556
MOD_GlcNHglycan 658 661 PF01048 0.730
MOD_GSK3_1 112 119 PF00069 0.760
MOD_GSK3_1 234 241 PF00069 0.633
MOD_GSK3_1 309 316 PF00069 0.671
MOD_GSK3_1 332 339 PF00069 0.583
MOD_GSK3_1 349 356 PF00069 0.663
MOD_GSK3_1 514 521 PF00069 0.667
MOD_GSK3_1 568 575 PF00069 0.568
MOD_N-GLC_1 165 170 PF02516 0.628
MOD_N-GLC_1 217 222 PF02516 0.607
MOD_N-GLC_1 381 386 PF02516 0.645
MOD_N-GLC_1 387 392 PF02516 0.517
MOD_NEK2_1 117 122 PF00069 0.618
MOD_NEK2_1 133 138 PF00069 0.542
MOD_NEK2_1 139 144 PF00069 0.675
MOD_NEK2_1 289 294 PF00069 0.379
MOD_NEK2_1 313 318 PF00069 0.676
MOD_NEK2_1 358 363 PF00069 0.635
MOD_NEK2_1 405 410 PF00069 0.564
MOD_NEK2_1 504 509 PF00069 0.618
MOD_NEK2_1 513 518 PF00069 0.570
MOD_PIKK_1 174 180 PF00454 0.603
MOD_PIKK_1 666 672 PF00454 0.694
MOD_PKA_2 405 411 PF00069 0.508
MOD_PKA_2 666 672 PF00069 0.742
MOD_Plk_1 165 171 PF00069 0.722
MOD_Plk_1 174 180 PF00069 0.554
MOD_Plk_1 289 295 PF00069 0.385
MOD_Plk_1 358 364 PF00069 0.638
MOD_Plk_1 387 393 PF00069 0.430
MOD_Plk_1 406 412 PF00069 0.572
MOD_Plk_4 336 342 PF00069 0.558
MOD_Plk_4 358 364 PF00069 0.759
MOD_Plk_4 456 462 PF00069 0.690
MOD_Plk_4 623 629 PF00069 0.544
MOD_ProDKin_1 25 31 PF00069 0.790
MOD_ProDKin_1 332 338 PF00069 0.625
MOD_ProDKin_1 453 459 PF00069 0.674
MOD_ProDKin_1 473 479 PF00069 0.577
TRG_DiLeu_BaEn_2 197 203 PF01217 0.580
TRG_DiLeu_BaLyEn_6 300 305 PF01217 0.590
TRG_ENDOCYTIC_2 158 161 PF00928 0.666
TRG_ENDOCYTIC_2 214 217 PF00928 0.587
TRG_ENDOCYTIC_2 247 250 PF00928 0.623
TRG_ENDOCYTIC_2 460 463 PF00928 0.703
TRG_ER_diArg_1 346 348 PF00400 0.599
TRG_ER_diArg_1 452 454 PF00400 0.707
TRG_Pf-PMV_PEXEL_1 248 253 PF00026 0.610

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3S7X2B5 Leishmania donovani 78% 100%
A4HH87 Leishmania braziliensis 78% 100%
A4I4D3 Leishmania infantum 78% 96%
E9ADT2 Leishmania major 88% 100%

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS