LeishMANIAdb
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RING-type domain-containing protein

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

Quick info

Protein:
RING-type domain-containing protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania mexicana
UniProt:
E9APF7_LEIMU
TriTrypDb:
LmxM.13.1330
Length:
496

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 3
GO:0110165 cellular anatomical entity 1 3

Expansion

Sequence features

E9APF7
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9APF7

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_NRD_NRD_1 420 422 PF00675 0.515
CLV_PCSK_FUR_1 417 421 PF00082 0.510
CLV_PCSK_KEX2_1 416 418 PF00082 0.543
CLV_PCSK_KEX2_1 419 421 PF00082 0.516
CLV_PCSK_PC1ET2_1 416 418 PF00082 0.555
CLV_PCSK_SKI1_1 192 196 PF00082 0.453
CLV_PCSK_SKI1_1 236 240 PF00082 0.657
CLV_PCSK_SKI1_1 33 37 PF00082 0.658
DEG_APCC_DBOX_1 67 75 PF00400 0.645
DEG_SCF_FBW7_1 409 415 PF00400 0.792
DEG_SPOP_SBC_1 193 197 PF00917 0.453
DEG_SPOP_SBC_1 397 401 PF00917 0.659
DOC_CKS1_1 409 414 PF01111 0.791
DOC_CYCLIN_yCln2_LP_2 465 471 PF00134 0.380
DOC_MAPK_gen_1 66 74 PF00069 0.645
DOC_MAPK_RevD_3 405 418 PF00069 0.749
DOC_PP4_FxxP_1 221 224 PF00568 0.453
DOC_PP4_FxxP_1 295 298 PF00568 0.757
DOC_USP7_MATH_1 13 17 PF00917 0.435
DOC_USP7_MATH_1 130 134 PF00917 0.695
DOC_USP7_MATH_1 194 198 PF00917 0.453
DOC_USP7_MATH_1 241 245 PF00917 0.506
DOC_USP7_MATH_1 257 261 PF00917 0.451
DOC_USP7_MATH_1 315 319 PF00917 0.680
DOC_USP7_MATH_1 393 397 PF00917 0.754
DOC_USP7_MATH_1 486 490 PF00917 0.512
DOC_USP7_UBL2_3 108 112 PF12436 0.726
DOC_WW_Pin1_4 154 159 PF00397 0.610
DOC_WW_Pin1_4 231 236 PF00397 0.546
DOC_WW_Pin1_4 252 257 PF00397 0.476
DOC_WW_Pin1_4 311 316 PF00397 0.712
DOC_WW_Pin1_4 328 333 PF00397 0.644
DOC_WW_Pin1_4 369 374 PF00397 0.696
DOC_WW_Pin1_4 408 413 PF00397 0.791
DOC_WW_Pin1_4 456 461 PF00397 0.506
DOC_WW_Pin1_4 50 55 PF00397 0.306
LIG_14-3-3_CanoR_1 131 140 PF00244 0.812
LIG_14-3-3_CanoR_1 192 202 PF00244 0.402
LIG_14-3-3_CanoR_1 357 367 PF00244 0.682
LIG_Actin_WH2_1 333 349 PF00022 0.557
LIG_Actin_WH2_2 334 349 PF00022 0.557
LIG_BRCT_BRCA1_1 275 279 PF00533 0.714
LIG_CaM_NSCaTE_8 483 490 PF13499 0.385
LIG_EH1_1 334 342 PF00400 0.646
LIG_eIF4E_1 335 341 PF01652 0.644
LIG_FHA_1 194 200 PF00498 0.326
LIG_FHA_1 259 265 PF00498 0.252
LIG_FHA_1 294 300 PF00498 0.725
LIG_FHA_1 409 415 PF00498 0.792
LIG_FHA_1 422 428 PF00498 0.648
LIG_FHA_1 488 494 PF00498 0.515
LIG_FHA_1 51 57 PF00498 0.486
LIG_FHA_2 474 480 PF00498 0.479
LIG_LIR_Apic_2 216 220 PF02991 0.484
LIG_LIR_Gen_1 204 210 PF02991 0.428
LIG_LIR_Gen_1 287 295 PF02991 0.728
LIG_LIR_Gen_1 324 335 PF02991 0.651
LIG_LIR_Nem_3 204 208 PF02991 0.428
LIG_LIR_Nem_3 260 265 PF02991 0.424
LIG_LIR_Nem_3 276 282 PF02991 0.570
LIG_LIR_Nem_3 287 292 PF02991 0.680
LIG_LIR_Nem_3 324 330 PF02991 0.652
LIG_LIR_Nem_3 441 447 PF02991 0.335
LIG_LIR_Nem_3 464 470 PF02991 0.524
LIG_LIR_Nem_3 476 481 PF02991 0.434
LIG_PDZ_Class_2 491 496 PF00595 0.523
LIG_Pex14_1 275 279 PF04695 0.667
LIG_SH2_CRK 161 165 PF00017 0.702
LIG_SH2_CRK 186 190 PF00017 0.492
LIG_SH2_CRK 217 221 PF00017 0.427
LIG_SH2_NCK_1 217 221 PF00017 0.427
LIG_SH2_STAT5 335 338 PF00017 0.649
LIG_SH2_STAT5 481 484 PF00017 0.520
LIG_SH3_2 342 347 PF14604 0.688
LIG_SH3_3 152 158 PF00018 0.613
LIG_SH3_3 250 256 PF00018 0.491
LIG_SH3_3 339 345 PF00018 0.726
LIG_SH3_3 389 395 PF00018 0.695
LIG_SH3_3 406 412 PF00018 0.749
LIG_SUMO_SIM_anti_2 489 495 PF11976 0.429
LIG_SUMO_SIM_par_1 195 204 PF11976 0.294
LIG_SUMO_SIM_par_1 467 473 PF11976 0.496
LIG_TRAF2_1 97 100 PF00917 0.748
LIG_WRC_WIRS_1 202 207 PF05994 0.389
LIG_WRC_WIRS_1 264 269 PF05994 0.453
LIG_WW_2 392 395 PF00397 0.614
MOD_CDK_SPK_2 231 236 PF00069 0.501
MOD_CDK_SPK_2 328 333 PF00069 0.644
MOD_CK1_1 106 112 PF00069 0.657
MOD_CK1_1 132 138 PF00069 0.694
MOD_CK1_1 201 207 PF00069 0.387
MOD_CK1_1 234 240 PF00069 0.525
MOD_CK1_1 246 252 PF00069 0.451
MOD_CK1_1 314 320 PF00069 0.627
MOD_CK1_1 396 402 PF00069 0.813
MOD_CK1_1 453 459 PF00069 0.440
MOD_CK1_1 461 467 PF00069 0.467
MOD_CK1_1 489 495 PF00069 0.515
MOD_CK2_1 357 363 PF00069 0.554
MOD_GlcNHglycan 15 18 PF01048 0.576
MOD_GlcNHglycan 19 23 PF01048 0.569
MOD_GlcNHglycan 239 242 PF01048 0.721
MOD_GlcNHglycan 269 272 PF01048 0.324
MOD_GlcNHglycan 306 309 PF01048 0.571
MOD_GlcNHglycan 395 398 PF01048 0.574
MOD_GlcNHglycan 401 404 PF01048 0.546
MOD_GlcNHglycan 456 459 PF01048 0.699
MOD_GSK3_1 129 136 PF00069 0.692
MOD_GSK3_1 150 157 PF00069 0.693
MOD_GSK3_1 194 201 PF00069 0.373
MOD_GSK3_1 237 244 PF00069 0.521
MOD_GSK3_1 263 270 PF00069 0.324
MOD_GSK3_1 306 313 PF00069 0.755
MOD_GSK3_1 322 329 PF00069 0.740
MOD_GSK3_1 357 364 PF00069 0.657
MOD_GSK3_1 369 376 PF00069 0.667
MOD_GSK3_1 377 384 PF00069 0.691
MOD_GSK3_1 393 400 PF00069 0.731
MOD_GSK3_1 408 415 PF00069 0.734
MOD_GSK3_1 449 456 PF00069 0.545
MOD_N-GLC_1 258 263 PF02516 0.596
MOD_N-GLC_1 304 309 PF02516 0.415
MOD_NEK2_1 174 179 PF00069 0.641
MOD_NEK2_1 18 23 PF00069 0.414
MOD_NEK2_1 247 252 PF00069 0.552
MOD_NEK2_1 267 272 PF00069 0.335
MOD_NEK2_1 322 327 PF00069 0.733
MOD_NEK2_1 336 341 PF00069 0.580
MOD_NEK2_1 426 431 PF00069 0.588
MOD_NEK2_1 449 454 PF00069 0.537
MOD_NEK2_2 243 248 PF00069 0.522
MOD_PIKK_1 134 140 PF00454 0.714
MOD_PIKK_1 293 299 PF00454 0.693
MOD_PIKK_1 315 321 PF00454 0.757
MOD_PKA_2 130 136 PF00069 0.738
MOD_PKA_2 356 362 PF00069 0.724
MOD_PKB_1 419 427 PF00069 0.737
MOD_Plk_1 258 264 PF00069 0.376
MOD_Plk_1 440 446 PF00069 0.389
MOD_Plk_4 139 145 PF00069 0.684
MOD_Plk_4 150 156 PF00069 0.660
MOD_Plk_4 201 207 PF00069 0.364
MOD_Plk_4 243 249 PF00069 0.511
MOD_Plk_4 26 32 PF00069 0.458
MOD_Plk_4 284 290 PF00069 0.637
MOD_Plk_4 322 328 PF00069 0.729
MOD_Plk_4 336 342 PF00069 0.593
MOD_Plk_4 489 495 PF00069 0.429
MOD_ProDKin_1 154 160 PF00069 0.606
MOD_ProDKin_1 231 237 PF00069 0.542
MOD_ProDKin_1 252 258 PF00069 0.473
MOD_ProDKin_1 311 317 PF00069 0.711
MOD_ProDKin_1 328 334 PF00069 0.644
MOD_ProDKin_1 369 375 PF00069 0.697
MOD_ProDKin_1 408 414 PF00069 0.791
MOD_ProDKin_1 456 462 PF00069 0.508
MOD_ProDKin_1 50 56 PF00069 0.306
MOD_SUMO_rev_2 29 38 PF00179 0.528
TRG_DiLeu_BaLyEn_6 422 427 PF01217 0.775
TRG_ENDOCYTIC_2 161 164 PF00928 0.758
TRG_ENDOCYTIC_2 186 189 PF00928 0.630
TRG_ENDOCYTIC_2 335 338 PF00928 0.649
TRG_ER_diArg_1 417 420 PF00400 0.723
TRG_NLS_MonoCore_2 415 420 PF00514 0.753
TRG_NLS_MonoExtC_3 415 420 PF00514 0.753

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I976 Leptomonas seymouri 43% 96%
A0A3Q8ICY4 Leishmania donovani 88% 100%
A4H7B6 Leishmania braziliensis 70% 100%
A4HVR1 Leishmania infantum 87% 100%
Q4QG21 Leishmania major 86% 99%

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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