LeishMANIAdb
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RRM domain-containing protein

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

Quick info

Protein:
RRM domain-containing protein
Gene product:
Nucleoporin NUP65, putative
Species:
Leishmania major
UniProt:
E9AEN8_LEIMA
TriTrypDb:
LmjF.35.0630 , LMJLV39_350012000 , LMJSD75_350011500 *
Length:
597

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:0016020 membrane 2 5
GO:0110165 cellular anatomical entity 1 5

Expansion

Sequence features

E9AEN8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AEN8

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 31 35 PF00656 0.545
CLV_NRD_NRD_1 12 14 PF00675 0.678
CLV_NRD_NRD_1 16 18 PF00675 0.720
CLV_NRD_NRD_1 197 199 PF00675 0.609
CLV_NRD_NRD_1 411 413 PF00675 0.546
CLV_NRD_NRD_1 445 447 PF00675 0.445
CLV_PCSK_FUR_1 13 17 PF00082 0.677
CLV_PCSK_FUR_1 195 199 PF00082 0.575
CLV_PCSK_FUR_1 443 447 PF00082 0.490
CLV_PCSK_KEX2_1 12 14 PF00082 0.678
CLV_PCSK_KEX2_1 15 17 PF00082 0.715
CLV_PCSK_KEX2_1 197 199 PF00082 0.609
CLV_PCSK_KEX2_1 411 413 PF00082 0.546
CLV_PCSK_KEX2_1 445 447 PF00082 0.448
CLV_PCSK_PC7_1 12 18 PF00082 0.735
CLV_PCSK_PC7_1 193 199 PF00082 0.562
CLV_PCSK_PC7_1 441 447 PF00082 0.452
CLV_PCSK_SKI1_1 198 202 PF00082 0.626
CLV_PCSK_SKI1_1 41 45 PF00082 0.678
CLV_PCSK_SKI1_1 445 449 PF00082 0.379
CLV_PCSK_SKI1_1 501 505 PF00082 0.471
DEG_APCC_DBOX_1 562 570 PF00400 0.647
DEG_Nend_Nbox_1 1 3 PF02207 0.435
DEG_SCF_FBW7_1 228 234 PF00400 0.456
DEG_SPOP_SBC_1 142 146 PF00917 0.443
DEG_SPOP_SBC_1 361 365 PF00917 0.437
DOC_ANK_TNKS_1 519 526 PF00023 0.670
DOC_CKS1_1 228 233 PF01111 0.456
DOC_CYCLIN_RxL_1 193 202 PF00134 0.368
DOC_CYCLIN_yCln2_LP_2 374 380 PF00134 0.318
DOC_MAPK_gen_1 12 22 PF00069 0.430
DOC_MAPK_gen_1 172 181 PF00069 0.515
DOC_MAPK_gen_1 501 509 PF00069 0.648
DOC_MAPK_gen_1 561 570 PF00069 0.620
DOC_MAPK_MEF2A_6 172 181 PF00069 0.452
DOC_MAPK_MEF2A_6 561 570 PF00069 0.626
DOC_MAPK_MEF2A_6 580 588 PF00069 0.281
DOC_PP1_SILK_1 37 42 PF00149 0.530
DOC_PP2B_LxvP_1 430 433 PF13499 0.703
DOC_PP4_FxxP_1 132 135 PF00568 0.300
DOC_PP4_FxxP_1 358 361 PF00568 0.451
DOC_SPAK_OSR1_1 379 383 PF12202 0.403
DOC_USP7_MATH_1 156 160 PF00917 0.475
DOC_USP7_MATH_1 215 219 PF00917 0.527
DOC_USP7_MATH_1 231 235 PF00917 0.473
DOC_USP7_MATH_1 243 247 PF00917 0.490
DOC_USP7_MATH_1 285 289 PF00917 0.498
DOC_USP7_MATH_1 294 298 PF00917 0.524
DOC_USP7_MATH_1 314 318 PF00917 0.479
DOC_USP7_MATH_1 35 39 PF00917 0.492
DOC_USP7_MATH_1 361 365 PF00917 0.437
DOC_USP7_MATH_1 397 401 PF00917 0.704
DOC_USP7_MATH_1 437 441 PF00917 0.702
DOC_USP7_MATH_1 496 500 PF00917 0.586
DOC_USP7_MATH_1 532 536 PF00917 0.746
DOC_USP7_MATH_1 67 71 PF00917 0.527
DOC_USP7_MATH_2 460 466 PF00917 0.669
DOC_WW_Pin1_4 131 136 PF00397 0.279
DOC_WW_Pin1_4 21 26 PF00397 0.549
DOC_WW_Pin1_4 227 232 PF00397 0.512
DOC_WW_Pin1_4 362 367 PF00397 0.479
DOC_WW_Pin1_4 428 433 PF00397 0.725
DOC_WW_Pin1_4 456 461 PF00397 0.623
LIG_14-3-3_CanoR_1 143 148 PF00244 0.446
LIG_14-3-3_CanoR_1 232 236 PF00244 0.534
LIG_14-3-3_CanoR_1 276 281 PF00244 0.516
LIG_14-3-3_CanoR_1 449 455 PF00244 0.630
LIG_14-3-3_CanoR_1 580 585 PF00244 0.403
LIG_Actin_WH2_2 389 407 PF00022 0.472
LIG_APCC_ABBAyCdc20_2 185 191 PF00400 0.425
LIG_BRCT_BRCA1_1 145 149 PF00533 0.437
LIG_BRCT_BRCA1_1 355 359 PF00533 0.450
LIG_eIF4E_1 581 587 PF01652 0.318
LIG_FHA_1 307 313 PF00498 0.451
LIG_FHA_1 34 40 PF00498 0.538
LIG_FHA_1 350 356 PF00498 0.477
LIG_FHA_1 369 375 PF00498 0.354
LIG_FHA_1 425 431 PF00498 0.709
LIG_FHA_1 85 91 PF00498 0.340
LIG_FHA_2 153 159 PF00498 0.458
LIG_FHA_2 281 287 PF00498 0.530
LIG_FHA_2 3 9 PF00498 0.445
LIG_FHA_2 536 542 PF00498 0.695
LIG_FHA_2 550 556 PF00498 0.607
LIG_FHA_2 71 77 PF00498 0.522
LIG_IBAR_NPY_1 493 495 PF08397 0.642
LIG_LIR_Apic_2 356 361 PF02991 0.452
LIG_LIR_Gen_1 126 136 PF02991 0.279
LIG_LIR_Gen_1 367 378 PF02991 0.427
LIG_LIR_Gen_1 387 397 PF02991 0.235
LIG_LIR_Gen_1 459 469 PF02991 0.614
LIG_LIR_Gen_1 487 496 PF02991 0.614
LIG_LIR_Gen_1 535 545 PF02991 0.688
LIG_LIR_Gen_1 585 594 PF02991 0.348
LIG_LIR_Gen_1 70 80 PF02991 0.525
LIG_LIR_Gen_1 86 96 PF02991 0.234
LIG_LIR_LC3C_4 176 181 PF02991 0.314
LIG_LIR_Nem_3 104 109 PF02991 0.191
LIG_LIR_Nem_3 126 132 PF02991 0.279
LIG_LIR_Nem_3 319 325 PF02991 0.534
LIG_LIR_Nem_3 367 373 PF02991 0.462
LIG_LIR_Nem_3 387 392 PF02991 0.193
LIG_LIR_Nem_3 462 466 PF02991 0.599
LIG_LIR_Nem_3 487 491 PF02991 0.609
LIG_LIR_Nem_3 535 540 PF02991 0.657
LIG_LIR_Nem_3 585 590 PF02991 0.348
LIG_LIR_Nem_3 70 75 PF02991 0.548
LIG_LIR_Nem_3 86 91 PF02991 0.234
LIG_MLH1_MIPbox_1 355 359 PF16413 0.450
LIG_PCNA_yPIPBox_3 74 84 PF02747 0.476
LIG_Pex14_1 488 492 PF04695 0.569
LIG_Pex14_1 577 581 PF04695 0.318
LIG_SH2_CRK 469 473 PF00017 0.611
LIG_SH2_CRK 581 585 PF00017 0.318
LIG_SH2_NCK_1 325 329 PF00017 0.512
LIG_SH2_STAP1 147 151 PF00017 0.375
LIG_SH2_STAT3 495 498 PF00017 0.678
LIG_SH2_STAT5 105 108 PF00017 0.346
LIG_SH2_STAT5 109 112 PF00017 0.316
LIG_SH2_STAT5 117 120 PF00017 0.271
LIG_SH2_STAT5 322 325 PF00017 0.424
LIG_SH2_STAT5 471 474 PF00017 0.652
LIG_SH2_STAT5 72 75 PF00017 0.528
LIG_SH3_1 470 476 PF00018 0.621
LIG_SH3_2 170 175 PF14604 0.502
LIG_SH3_2 429 434 PF14604 0.706
LIG_SH3_3 167 173 PF00018 0.543
LIG_SH3_3 260 266 PF00018 0.518
LIG_SH3_3 275 281 PF00018 0.519
LIG_SH3_3 293 299 PF00018 0.485
LIG_SH3_3 426 432 PF00018 0.702
LIG_SH3_3 470 476 PF00018 0.621
LIG_SUMO_SIM_anti_2 176 181 PF11976 0.351
LIG_SUMO_SIM_par_1 380 385 PF11976 0.321
LIG_SUMO_SIM_par_1 97 104 PF11976 0.279
LIG_TYR_ITIM 467 472 PF00017 0.599
LIG_WRC_WIRS_1 463 468 PF05994 0.656
LIG_WW_3 172 176 PF00397 0.487
LIG_WW_3 431 435 PF00397 0.704
MOD_CDC14_SPxK_1 431 434 PF00782 0.704
MOD_CDK_SPK_2 227 232 PF00069 0.475
MOD_CDK_SPxK_1 428 434 PF00069 0.707
MOD_CDK_SPxxK_3 362 369 PF00069 0.484
MOD_CK1_1 119 125 PF00069 0.334
MOD_CK1_1 145 151 PF00069 0.440
MOD_CK1_1 159 165 PF00069 0.437
MOD_CK1_1 238 244 PF00069 0.515
MOD_CK1_1 279 285 PF00069 0.514
MOD_CK1_1 290 296 PF00069 0.532
MOD_CK1_1 297 303 PF00069 0.470
MOD_CK1_1 305 311 PF00069 0.556
MOD_CK1_1 342 348 PF00069 0.464
MOD_CK1_1 364 370 PF00069 0.442
MOD_CK1_1 535 541 PF00069 0.650
MOD_CK1_1 582 588 PF00069 0.332
MOD_CK1_1 70 76 PF00069 0.502
MOD_CK2_1 152 158 PF00069 0.453
MOD_CK2_1 280 286 PF00069 0.522
MOD_CK2_1 456 462 PF00069 0.621
MOD_CK2_1 535 541 PF00069 0.692
MOD_CK2_1 549 555 PF00069 0.609
MOD_CK2_1 70 76 PF00069 0.531
MOD_CMANNOS 386 389 PF00535 0.403
MOD_GlcNHglycan 122 125 PF01048 0.485
MOD_GlcNHglycan 233 236 PF01048 0.771
MOD_GlcNHglycan 240 244 PF01048 0.851
MOD_GlcNHglycan 272 275 PF01048 0.768
MOD_GlcNHglycan 292 295 PF01048 0.785
MOD_GlcNHglycan 296 299 PF01048 0.724
MOD_GlcNHglycan 304 307 PF01048 0.697
MOD_GlcNHglycan 31 34 PF01048 0.709
MOD_GlcNHglycan 316 319 PF01048 0.770
MOD_GlcNHglycan 344 347 PF01048 0.647
MOD_GlcNHglycan 366 369 PF01048 0.636
MOD_GlcNHglycan 399 402 PF01048 0.480
MOD_GlcNHglycan 456 459 PF01048 0.422
MOD_GlcNHglycan 514 517 PF01048 0.471
MOD_GlcNHglycan 91 94 PF01048 0.540
MOD_GSK3_1 116 123 PF00069 0.319
MOD_GSK3_1 141 148 PF00069 0.372
MOD_GSK3_1 152 159 PF00069 0.436
MOD_GSK3_1 210 217 PF00069 0.509
MOD_GSK3_1 223 230 PF00069 0.543
MOD_GSK3_1 231 238 PF00069 0.492
MOD_GSK3_1 239 246 PF00069 0.460
MOD_GSK3_1 270 277 PF00069 0.549
MOD_GSK3_1 280 287 PF00069 0.483
MOD_GSK3_1 29 36 PF00069 0.482
MOD_GSK3_1 290 297 PF00069 0.492
MOD_GSK3_1 302 309 PF00069 0.522
MOD_GSK3_1 349 356 PF00069 0.399
MOD_GSK3_1 360 367 PF00069 0.421
MOD_GSK3_1 424 431 PF00069 0.739
MOD_GSK3_1 532 539 PF00069 0.683
MOD_GSK3_1 549 556 PF00069 0.567
MOD_NEK2_1 118 123 PF00069 0.341
MOD_NEK2_1 239 244 PF00069 0.524
MOD_NEK2_1 292 297 PF00069 0.564
MOD_NEK2_1 340 345 PF00069 0.536
MOD_NEK2_1 349 354 PF00069 0.440
MOD_NEK2_1 384 389 PF00069 0.403
MOD_NEK2_1 503 508 PF00069 0.609
MOD_NEK2_1 83 88 PF00069 0.446
MOD_NEK2_2 156 161 PF00069 0.480
MOD_NEK2_2 496 501 PF00069 0.628
MOD_PIKK_1 204 210 PF00454 0.482
MOD_PIKK_1 285 291 PF00454 0.510
MOD_PIKK_1 424 430 PF00454 0.749
MOD_PIKK_1 553 559 PF00454 0.591
MOD_PIKK_1 67 73 PF00454 0.498
MOD_PKA_2 142 148 PF00069 0.440
MOD_PKA_2 231 237 PF00069 0.553
MOD_PKA_2 243 249 PF00069 0.482
MOD_PKA_2 270 276 PF00069 0.578
MOD_PKA_2 368 374 PF00069 0.521
MOD_PKA_2 448 454 PF00069 0.669
MOD_PKA_2 549 555 PF00069 0.706
MOD_PKA_2 579 585 PF00069 0.403
MOD_Plk_4 35 41 PF00069 0.534
MOD_Plk_4 350 356 PF00069 0.499
MOD_Plk_4 462 468 PF00069 0.621
MOD_Plk_4 503 509 PF00069 0.610
MOD_Plk_4 52 58 PF00069 0.418
MOD_Plk_4 582 588 PF00069 0.318
MOD_Plk_4 84 90 PF00069 0.264
MOD_ProDKin_1 131 137 PF00069 0.279
MOD_ProDKin_1 21 27 PF00069 0.549
MOD_ProDKin_1 227 233 PF00069 0.513
MOD_ProDKin_1 362 368 PF00069 0.473
MOD_ProDKin_1 428 434 PF00069 0.727
MOD_ProDKin_1 456 462 PF00069 0.621
TRG_DiLeu_BaEn_1 565 570 PF01217 0.618
TRG_DiLeu_BaEn_2 461 467 PF01217 0.601
TRG_DiLeu_BaLyEn_6 260 265 PF01217 0.519
TRG_DiLeu_BaLyEn_6 498 503 PF01217 0.644
TRG_ENDOCYTIC_2 117 120 PF00928 0.339
TRG_ENDOCYTIC_2 129 132 PF00928 0.236
TRG_ENDOCYTIC_2 375 378 PF00928 0.318
TRG_ENDOCYTIC_2 463 466 PF00928 0.595
TRG_ENDOCYTIC_2 469 472 PF00928 0.610
TRG_ENDOCYTIC_2 581 584 PF00928 0.318
TRG_ENDOCYTIC_2 72 75 PF00928 0.528
TRG_ER_diArg_1 12 15 PF00400 0.484
TRG_ER_diArg_1 195 198 PF00400 0.397
TRG_ER_diArg_1 442 445 PF00400 0.711
TRG_ER_diArg_1 560 563 PF00400 0.584
TRG_Pf-PMV_PEXEL_1 198 202 PF00026 0.615
TRG_Pf-PMV_PEXEL_1 434 438 PF00026 0.500
TRG_Pf-PMV_PEXEL_1 501 505 PF00026 0.471

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1HRZ6 Leptomonas seymouri 47% 100%
A0A3S7X8T0 Leishmania donovani 90% 100%
A4HM96 Leishmania braziliensis 77% 100%
A4IAW0 Leishmania infantum 91% 100%
E9B5U4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 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