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 braziliensis
UniProt:
A4HH87_LEIBR
TriTrypDb:
LbrM.29.0820 , LBRM2903_290014600 *
Length:
652

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: 6
NetGPI no yes: 0, no: 6
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

A4HH87
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HH87

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 212 216 PF00656 0.468
CLV_NRD_NRD_1 271 273 PF00675 0.594
CLV_NRD_NRD_1 444 446 PF00675 0.643
CLV_NRD_NRD_1 649 651 PF00675 0.565
CLV_PCSK_KEX2_1 271 273 PF00082 0.594
CLV_PCSK_KEX2_1 444 446 PF00082 0.585
CLV_PCSK_KEX2_1 649 651 PF00082 0.570
CLV_PCSK_SKI1_1 239 243 PF00082 0.599
CLV_PCSK_SKI1_1 414 418 PF00082 0.522
DEG_APCC_DBOX_1 238 246 PF00400 0.598
DEG_APCC_DBOX_1 270 278 PF00400 0.575
DEG_SPOP_SBC_1 233 237 PF00917 0.635
DEG_SPOP_SBC_1 469 473 PF00917 0.676
DEG_SPOP_SBC_1 485 489 PF00917 0.511
DOC_CDC14_PxL_1 451 459 PF14671 0.675
DOC_CYCLIN_RxL_1 409 418 PF00134 0.472
DOC_CYCLIN_yCln2_LP_2 353 356 PF00134 0.634
DOC_MAPK_gen_1 202 208 PF00069 0.563
DOC_PP1_RVXF_1 161 168 PF00149 0.503
DOC_PP2B_LxvP_1 353 356 PF13499 0.634
DOC_PP2B_LxvP_1 64 67 PF13499 0.506
DOC_PP4_FxxP_1 452 455 PF00568 0.676
DOC_PP4_FxxP_1 521 524 PF00568 0.598
DOC_PP4_FxxP_1 60 63 PF00568 0.504
DOC_PP4_FxxP_1 70 73 PF00568 0.494
DOC_USP7_MATH_1 115 119 PF00917 0.594
DOC_USP7_MATH_1 225 229 PF00917 0.625
DOC_USP7_MATH_1 231 235 PF00917 0.557
DOC_USP7_MATH_1 27 31 PF00917 0.668
DOC_USP7_MATH_1 318 322 PF00917 0.728
DOC_USP7_MATH_1 356 360 PF00917 0.679
DOC_USP7_MATH_1 446 450 PF00917 0.591
DOC_USP7_MATH_1 458 462 PF00917 0.489
DOC_USP7_MATH_1 465 469 PF00917 0.543
DOC_USP7_MATH_1 586 590 PF00917 0.725
DOC_USP7_MATH_1 635 639 PF00917 0.699
DOC_WW_Pin1_4 227 232 PF00397 0.482
DOC_WW_Pin1_4 25 30 PF00397 0.690
DOC_WW_Pin1_4 323 328 PF00397 0.653
DOC_WW_Pin1_4 34 39 PF00397 0.611
DOC_WW_Pin1_4 444 449 PF00397 0.647
DOC_WW_Pin1_4 460 465 PF00397 0.552
DOC_WW_Pin1_4 559 564 PF00397 0.528
LIG_14-3-3_CanoR_1 437 443 PF00244 0.565
LIG_Actin_WH2_2 346 363 PF00022 0.673
LIG_Actin_WH2_2 382 399 PF00022 0.557
LIG_APCC_ABBAyCdc20_2 191 197 PF00400 0.539
LIG_BIR_II_1 1 5 PF00653 0.653
LIG_BRCT_BRCA1_1 448 452 PF00533 0.660
LIG_FHA_1 114 120 PF00498 0.616
LIG_FHA_1 169 175 PF00498 0.580
LIG_FHA_1 471 477 PF00498 0.606
LIG_FHA_1 486 492 PF00498 0.649
LIG_FHA_2 345 351 PF00498 0.507
LIG_FHA_2 448 454 PF00498 0.650
LIG_GBD_Chelix_1 331 339 PF00786 0.558
LIG_Integrin_isoDGR_2 373 375 PF01839 0.512
LIG_LIR_Apic_2 449 455 PF02991 0.670
LIG_LIR_Apic_2 518 524 PF02991 0.672
LIG_LIR_Gen_1 164 174 PF02991 0.506
LIG_LIR_Gen_1 326 335 PF02991 0.575
LIG_LIR_Nem_3 164 170 PF02991 0.501
LIG_LIR_Nem_3 235 241 PF02991 0.552
LIG_LIR_Nem_3 326 331 PF02991 0.606
LIG_LIR_Nem_3 449 454 PF02991 0.647
LIG_MLH1_MIPbox_1 448 452 PF16413 0.660
LIG_MYND_1 604 608 PF01753 0.529
LIG_NRP_CendR_1 649 652 PF00754 0.719
LIG_SH2_CRK 149 153 PF00017 0.459
LIG_SH2_CRK 238 242 PF00017 0.608
LIG_SH2_GRB2like 207 210 PF00017 0.571
LIG_SH2_STAP1 287 291 PF00017 0.479
LIG_SH2_STAT3 147 150 PF00017 0.492
LIG_SH2_STAT5 205 208 PF00017 0.572
LIG_SH2_STAT5 451 454 PF00017 0.632
LIG_SH3_3 136 142 PF00018 0.699
LIG_SH3_3 288 294 PF00018 0.480
LIG_SH3_3 452 458 PF00018 0.673
LIG_SH3_3 598 604 PF00018 0.769
LIG_SH3_3 605 611 PF00018 0.641
LIG_UBA3_1 241 249 PF00899 0.587
LIG_WRC_WIRS_1 190 195 PF05994 0.574
LIG_WW_2 455 458 PF00397 0.668
MOD_CK1_1 113 119 PF00069 0.609
MOD_CK1_1 168 174 PF00069 0.587
MOD_CK1_1 229 235 PF00069 0.591
MOD_CK1_1 344 350 PF00069 0.575
MOD_CK1_1 447 453 PF00069 0.630
MOD_CK1_1 468 474 PF00069 0.583
MOD_CK1_1 613 619 PF00069 0.549
MOD_CK2_1 344 350 PF00069 0.429
MOD_GlcNHglycan 215 218 PF01048 0.572
MOD_GlcNHglycan 223 226 PF01048 0.669
MOD_GlcNHglycan 306 309 PF01048 0.602
MOD_GlcNHglycan 343 346 PF01048 0.516
MOD_GlcNHglycan 467 470 PF01048 0.798
MOD_GlcNHglycan 488 491 PF01048 0.557
MOD_GlcNHglycan 498 501 PF01048 0.644
MOD_GlcNHglycan 52 55 PF01048 0.619
MOD_GlcNHglycan 521 524 PF01048 0.545
MOD_GlcNHglycan 588 591 PF01048 0.663
MOD_GlcNHglycan 612 615 PF01048 0.541
MOD_GlcNHglycan 637 640 PF01048 0.755
MOD_GlcNHglycan 64 67 PF01048 0.506
MOD_GSK3_1 101 108 PF00069 0.702
MOD_GSK3_1 110 117 PF00069 0.703
MOD_GSK3_1 221 228 PF00069 0.644
MOD_GSK3_1 229 236 PF00069 0.564
MOD_GSK3_1 28 35 PF00069 0.727
MOD_GSK3_1 300 307 PF00069 0.616
MOD_GSK3_1 340 347 PF00069 0.417
MOD_GSK3_1 465 472 PF00069 0.678
MOD_GSK3_1 474 481 PF00069 0.533
MOD_GSK3_1 515 522 PF00069 0.766
MOD_GSK3_1 83 90 PF00069 0.507
MOD_N-GLC_1 156 161 PF02516 0.563
MOD_N-GLC_1 208 213 PF02516 0.576
MOD_N-GLC_2 310 312 PF02516 0.511
MOD_NEK2_1 111 116 PF00069 0.667
MOD_NEK2_1 133 138 PF00069 0.735
MOD_NEK2_1 304 309 PF00069 0.772
MOD_NEK2_1 349 354 PF00069 0.656
MOD_NEK2_1 396 401 PF00069 0.639
MOD_NEK2_1 474 479 PF00069 0.587
MOD_NEK2_1 50 55 PF00069 0.497
MOD_NEK2_1 542 547 PF00069 0.500
MOD_NEK2_2 356 361 PF00069 0.579
MOD_PIKK_1 165 171 PF00454 0.573
MOD_PIKK_1 458 464 PF00454 0.528
MOD_PKA_2 396 402 PF00069 0.491
MOD_PKA_2 645 651 PF00069 0.714
MOD_Plk_1 156 162 PF00069 0.561
MOD_Plk_1 165 171 PF00069 0.453
MOD_Plk_1 349 355 PF00069 0.607
MOD_Plk_1 397 403 PF00069 0.609
MOD_Plk_4 349 355 PF00069 0.662
MOD_Plk_4 438 444 PF00069 0.529
MOD_Plk_4 447 453 PF00069 0.668
MOD_Plk_4 613 619 PF00069 0.528
MOD_ProDKin_1 227 233 PF00069 0.482
MOD_ProDKin_1 25 31 PF00069 0.693
MOD_ProDKin_1 323 329 PF00069 0.649
MOD_ProDKin_1 34 40 PF00069 0.607
MOD_ProDKin_1 444 450 PF00069 0.648
MOD_ProDKin_1 460 466 PF00069 0.555
MOD_ProDKin_1 559 565 PF00069 0.529
TRG_DiLeu_BaEn_2 188 194 PF01217 0.475
TRG_DiLeu_BaLyEn_6 291 296 PF01217 0.568
TRG_ENDOCYTIC_2 149 152 PF00928 0.542
TRG_ENDOCYTIC_2 205 208 PF00928 0.572
TRG_ENDOCYTIC_2 238 241 PF00928 0.540
TRG_ENDOCYTIC_2 451 454 PF00928 0.798
TRG_ER_diArg_1 443 445 PF00400 0.648
TRG_ER_diArg_1 649 652 PF00400 0.570
TRG_Pf-PMV_PEXEL_1 239 244 PF00026 0.597

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3R7L5N2 Trypanosoma rangeli 32% 100%
A0A3S7X2B5 Leishmania donovani 81% 99%
A4I4D3 Leishmania infantum 78% 93%
E9ADT2 Leishmania major 82% 100%
E9ALZ8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 78% 97%

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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