LeishMANIAdb
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Stealth_CR3 domain-containing protein

Quick info Annotations Function or PPIs Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Stealth_CR3 domain-containing protein
Gene product:
Protein of unknown function (DUF3184), putative
Species:
Leishmania braziliensis
UniProt:
A4H8N0_LEIBR
TriTrypDb:
LbrM.16.1070 , LBRM2903_160018200 *
Length:
788

Annotations

LeishMANIAdb annotations

N-acetylglucosamine-1-phosphotransferase homologous protein. Assumed to be a type II TM protein like its distant relatives.. Signal-anchored glycan biogenesis protein essential for mannose 6-P generation (lysosomal signal for the Metazoan hosts). Family only expended in Leishmaniids.. Localization: Golgi (by homology)

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. yes yes: 120
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: 32
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 34
NetGPI no yes: 0, no: 34
Cellular components
Term Name Level Count
GO:0016020 membrane 2 18
GO:0110165 cellular anatomical entity 1 25
GO:0005794 Golgi apparatus 5 9
GO:0043226 organelle 2 9
GO:0043227 membrane-bounded organelle 3 9
GO:0043229 intracellular organelle 3 9
GO:0043231 intracellular membrane-bounded organelle 4 9

Expansion

Sequence features

A4H8N0
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4H8N0

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 33
GO:0016740 transferase activity 2 33
GO:0016772 transferase activity, transferring phosphorus-containing groups 3 11

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 155 159 PF00656 0.427
CLV_C14_Caspase3-7 333 337 PF00656 0.586
CLV_NRD_NRD_1 126 128 PF00675 0.711
CLV_NRD_NRD_1 220 222 PF00675 0.744
CLV_NRD_NRD_1 277 279 PF00675 0.610
CLV_NRD_NRD_1 29 31 PF00675 0.476
CLV_NRD_NRD_1 477 479 PF00675 0.589
CLV_NRD_NRD_1 610 612 PF00675 0.618
CLV_NRD_NRD_1 9 11 PF00675 0.420
CLV_PCSK_FUR_1 475 479 PF00082 0.541
CLV_PCSK_FUR_1 608 612 PF00082 0.484
CLV_PCSK_KEX2_1 222 224 PF00082 0.584
CLV_PCSK_KEX2_1 277 279 PF00082 0.601
CLV_PCSK_KEX2_1 29 31 PF00082 0.489
CLV_PCSK_KEX2_1 477 479 PF00082 0.652
CLV_PCSK_KEX2_1 610 612 PF00082 0.522
CLV_PCSK_KEX2_1 9 11 PF00082 0.441
CLV_PCSK_PC1ET2_1 222 224 PF00082 0.534
CLV_PCSK_SKI1_1 190 194 PF00082 0.668
CLV_PCSK_SKI1_1 339 343 PF00082 0.825
CLV_PCSK_SKI1_1 393 397 PF00082 0.751
CLV_PCSK_SKI1_1 477 481 PF00082 0.566
CLV_PCSK_SKI1_1 532 536 PF00082 0.586
CLV_PCSK_SKI1_1 613 617 PF00082 0.597
CLV_PCSK_SKI1_1 754 758 PF00082 0.734
DEG_APCC_DBOX_1 305 313 PF00400 0.535
DEG_SCF_FBW7_2 658 665 PF00400 0.378
DEG_SPOP_SBC_1 544 548 PF00917 0.391
DEG_SPOP_SBC_1 557 561 PF00917 0.412
DOC_CKS1_1 761 766 PF01111 0.548
DOC_CYCLIN_RxL_1 474 482 PF00134 0.355
DOC_CYCLIN_yCln2_LP_2 615 621 PF00134 0.481
DOC_MAPK_gen_1 277 285 PF00069 0.386
DOC_MAPK_gen_1 317 326 PF00069 0.502
DOC_MAPK_gen_1 391 400 PF00069 0.531
DOC_MAPK_gen_1 608 617 PF00069 0.480
DOC_MAPK_HePTP_8 757 769 PF00069 0.534
DOC_MAPK_MEF2A_6 393 402 PF00069 0.525
DOC_MAPK_MEF2A_6 610 619 PF00069 0.481
DOC_MAPK_MEF2A_6 683 692 PF00069 0.358
DOC_MAPK_MEF2A_6 760 769 PF00069 0.544
DOC_PP2B_LxvP_1 615 618 PF13499 0.481
DOC_PP4_FxxP_1 761 764 PF00568 0.571
DOC_USP7_MATH_1 15 19 PF00917 0.589
DOC_USP7_MATH_1 270 274 PF00917 0.316
DOC_USP7_MATH_1 34 38 PF00917 0.625
DOC_USP7_MATH_1 353 357 PF00917 0.647
DOC_USP7_MATH_1 544 548 PF00917 0.391
DOC_USP7_MATH_1 686 690 PF00917 0.357
DOC_USP7_MATH_1 8 12 PF00917 0.625
DOC_USP7_MATH_1 97 101 PF00917 0.451
DOC_USP7_UBL2_3 679 683 PF12436 0.347
DOC_WW_Pin1_4 126 131 PF00397 0.489
DOC_WW_Pin1_4 190 195 PF00397 0.482
DOC_WW_Pin1_4 324 329 PF00397 0.535
DOC_WW_Pin1_4 658 663 PF00397 0.425
DOC_WW_Pin1_4 760 765 PF00397 0.530
LIG_14-3-3_CanoR_1 14 20 PF00244 0.590
LIG_14-3-3_CanoR_1 267 275 PF00244 0.333
LIG_14-3-3_CanoR_1 306 310 PF00244 0.489
LIG_14-3-3_CanoR_1 362 367 PF00244 0.563
LIG_14-3-3_CanoR_1 377 381 PF00244 0.374
LIG_14-3-3_CanoR_1 393 402 PF00244 0.340
LIG_14-3-3_CanoR_1 478 484 PF00244 0.476
LIG_14-3-3_CanoR_1 512 517 PF00244 0.443
LIG_14-3-3_CanoR_1 567 575 PF00244 0.469
LIG_14-3-3_CanoR_1 590 595 PF00244 0.323
LIG_Actin_WH2_2 347 364 PF00022 0.625
LIG_AP2alpha_1 596 600 PF02296 0.284
LIG_APCC_ABBA_1 666 671 PF00400 0.373
LIG_APCC_ABBA_1 688 693 PF00400 0.341
LIG_BIR_II_1 1 5 PF00653 0.657
LIG_BRCT_BRCA1_1 215 219 PF00533 0.341
LIG_BRCT_BRCA1_1 258 262 PF00533 0.355
LIG_BRCT_BRCA1_1 48 52 PF00533 0.259
LIG_BRCT_BRCA1_1 537 541 PF00533 0.364
LIG_BRCT_BRCA1_1 592 596 PF00533 0.284
LIG_BRCT_BRCA1_1 632 636 PF00533 0.497
LIG_BRCT_BRCA1_1 71 75 PF00533 0.429
LIG_BRCT_BRCA1_1 76 80 PF00533 0.431
LIG_BRCT_BRCA1_1 99 103 PF00533 0.451
LIG_eIF4E_1 467 473 PF01652 0.411
LIG_FHA_1 177 183 PF00498 0.430
LIG_FHA_1 19 25 PF00498 0.556
LIG_FHA_1 256 262 PF00498 0.378
LIG_FHA_1 288 294 PF00498 0.513
LIG_FHA_1 300 306 PF00498 0.525
LIG_FHA_1 558 564 PF00498 0.383
LIG_FHA_1 653 659 PF00498 0.384
LIG_FHA_1 715 721 PF00498 0.369
LIG_FHA_1 731 737 PF00498 0.339
LIG_FHA_2 191 197 PF00498 0.457
LIG_FHA_2 331 337 PF00498 0.580
LIG_FHA_2 521 527 PF00498 0.402
LIG_FHA_2 772 778 PF00498 0.460
LIG_Integrin_RGD_1 438 440 PF01839 0.556
LIG_LIR_Apic_2 242 247 PF02991 0.414
LIG_LIR_Gen_1 199 208 PF02991 0.429
LIG_LIR_Gen_1 269 275 PF02991 0.339
LIG_LIR_Gen_1 49 58 PF02991 0.266
LIG_LIR_Gen_1 493 502 PF02991 0.404
LIG_LIR_Gen_1 598 605 PF02991 0.289
LIG_LIR_Gen_1 763 773 PF02991 0.501
LIG_LIR_Nem_3 187 192 PF02991 0.367
LIG_LIR_Nem_3 196 201 PF02991 0.412
LIG_LIR_Nem_3 205 211 PF02991 0.433
LIG_LIR_Nem_3 269 274 PF02991 0.340
LIG_LIR_Nem_3 415 421 PF02991 0.440
LIG_LIR_Nem_3 452 458 PF02991 0.313
LIG_LIR_Nem_3 474 479 PF02991 0.422
LIG_LIR_Nem_3 49 53 PF02991 0.266
LIG_LIR_Nem_3 493 498 PF02991 0.402
LIG_LIR_Nem_3 598 603 PF02991 0.384
LIG_LIR_Nem_3 614 619 PF02991 0.391
LIG_LIR_Nem_3 633 639 PF02991 0.306
LIG_NRBOX 256 262 PF00104 0.360
LIG_PCNA_yPIPBox_3 277 286 PF02747 0.421
LIG_Pex14_1 592 596 PF04695 0.284
LIG_Pex14_2 52 56 PF04695 0.282
LIG_Pex14_2 537 541 PF04695 0.364
LIG_Pex14_2 596 600 PF04695 0.284
LIG_Pex14_2 76 80 PF04695 0.439
LIG_PTB_Apo_2 400 407 PF02174 0.508
LIG_PTB_Apo_2 731 738 PF02174 0.471
LIG_PTB_Phospho_1 400 406 PF10480 0.510
LIG_PTB_Phospho_1 731 737 PF10480 0.476
LIG_SH2_CRK 208 212 PF00017 0.510
LIG_SH2_CRK 244 248 PF00017 0.417
LIG_SH2_CRK 704 708 PF00017 0.397
LIG_SH2_GRB2like 401 404 PF00017 0.511
LIG_SH2_GRB2like 737 740 PF00017 0.471
LIG_SH2_NCK_1 165 169 PF00017 0.409
LIG_SH2_NCK_1 244 248 PF00017 0.408
LIG_SH2_STAP1 20 24 PF00017 0.544
LIG_SH2_STAP1 576 580 PF00017 0.481
LIG_SH2_STAT3 467 470 PF00017 0.319
LIG_SH2_STAT5 20 23 PF00017 0.571
LIG_SH2_STAT5 239 242 PF00017 0.439
LIG_SH2_STAT5 244 247 PF00017 0.465
LIG_SH2_STAT5 406 409 PF00017 0.502
LIG_SH2_STAT5 467 470 PF00017 0.479
LIG_SH2_STAT5 584 587 PF00017 0.450
LIG_SH2_STAT5 639 642 PF00017 0.515
LIG_SH2_STAT5 737 740 PF00017 0.468
LIG_SH2_STAT5 766 769 PF00017 0.573
LIG_SH3_3 171 177 PF00018 0.507
LIG_SH3_3 322 328 PF00018 0.330
LIG_SUMO_SIM_anti_2 202 209 PF11976 0.319
LIG_SUMO_SIM_par_1 231 236 PF11976 0.379
LIG_SUMO_SIM_par_1 322 327 PF11976 0.527
LIG_TYR_ITIM 206 211 PF00017 0.476
LIG_UBA3_1 232 237 PF00899 0.363
LIG_UBA3_1 494 501 PF00899 0.428
LIG_WRC_WIRS_1 207 212 PF05994 0.497
LIG_WRC_WIRS_1 47 52 PF05994 0.262
LIG_WRC_WIRS_1 753 758 PF05994 0.328
LIG_WRC_WIRS_1 98 103 PF05994 0.437
MOD_CDC14_SPxK_1 3 6 PF00782 0.641
MOD_CDK_SPxK_1 126 132 PF00069 0.444
MOD_CDK_SPxK_1 658 664 PF00069 0.376
MOD_CK1_1 18 24 PF00069 0.547
MOD_CK1_1 2 8 PF00069 0.638
MOD_CK1_1 242 248 PF00069 0.447
MOD_CK1_1 255 261 PF00069 0.379
MOD_CK1_1 266 272 PF00069 0.335
MOD_CK1_1 308 314 PF00069 0.507
MOD_CK1_1 356 362 PF00069 0.618
MOD_CK1_1 555 561 PF00069 0.432
MOD_CK1_1 69 75 PF00069 0.426
MOD_CK1_1 87 93 PF00069 0.497
MOD_CK2_1 190 196 PF00069 0.500
MOD_CK2_1 245 251 PF00069 0.475
MOD_CK2_1 441 447 PF00069 0.424
MOD_CK2_1 479 485 PF00069 0.381
MOD_CK2_1 511 517 PF00069 0.426
MOD_CK2_1 520 526 PF00069 0.409
MOD_CK2_1 545 551 PF00069 0.382
MOD_CK2_1 559 565 PF00069 0.375
MOD_CK2_1 742 748 PF00069 0.507
MOD_CK2_1 771 777 PF00069 0.456
MOD_CMANNOS 83 86 PF00535 0.640
MOD_Cter_Amidation 27 30 PF01082 0.431
MOD_Cter_Amidation 275 278 PF01082 0.556
MOD_GlcNHglycan 158 161 PF01048 0.631
MOD_GlcNHglycan 241 244 PF01048 0.612
MOD_GlcNHglycan 356 359 PF01048 0.780
MOD_GlcNHglycan 631 635 PF01048 0.485
MOD_GlcNHglycan 76 79 PF01048 0.694
MOD_GlcNHglycan 87 90 PF01048 0.705
MOD_GSK3_1 184 191 PF00069 0.344
MOD_GSK3_1 247 254 PF00069 0.530
MOD_GSK3_1 266 273 PF00069 0.330
MOD_GSK3_1 421 428 PF00069 0.530
MOD_GSK3_1 552 559 PF00069 0.430
MOD_GSK3_1 65 72 PF00069 0.427
MOD_GSK3_1 84 91 PF00069 0.488
MOD_LATS_1 360 366 PF00433 0.575
MOD_N-GLC_1 211 216 PF02516 0.740
MOD_N-GLC_1 255 260 PF02516 0.573
MOD_N-GLC_1 287 292 PF02516 0.598
MOD_N-GLC_1 393 398 PF02516 0.742
MOD_N-GLC_1 544 549 PF02516 0.584
MOD_N-GLC_1 555 560 PF02516 0.621
MOD_N-GLC_1 686 691 PF02516 0.515
MOD_NEK2_1 188 193 PF00069 0.342
MOD_NEK2_1 286 291 PF00069 0.441
MOD_NEK2_1 305 310 PF00069 0.489
MOD_NEK2_1 354 359 PF00069 0.620
MOD_NEK2_1 361 366 PF00069 0.511
MOD_NEK2_1 479 484 PF00069 0.444
MOD_NEK2_1 76 81 PF00069 0.475
MOD_NEK2_2 15 20 PF00069 0.574
MOD_NEK2_2 686 691 PF00069 0.344
MOD_PK_1 590 596 PF00069 0.287
MOD_PKA_2 150 156 PF00069 0.468
MOD_PKA_2 266 272 PF00069 0.332
MOD_PKA_2 299 305 PF00069 0.538
MOD_PKA_2 354 360 PF00069 0.623
MOD_PKA_2 361 367 PF00069 0.502
MOD_PKA_2 376 382 PF00069 0.364
MOD_PKA_2 511 517 PF00069 0.451
MOD_PKA_2 566 572 PF00069 0.386
MOD_PKA_2 714 720 PF00069 0.353
MOD_PKA_2 8 14 PF00069 0.629
MOD_PKA_2 84 90 PF00069 0.498
MOD_PKB_1 391 399 PF00069 0.459
MOD_PKB_1 508 516 PF00069 0.428
MOD_Plk_1 255 261 PF00069 0.361
MOD_Plk_1 393 399 PF00069 0.461
MOD_Plk_1 544 550 PF00069 0.379
MOD_Plk_1 65 71 PF00069 0.408
MOD_Plk_1 686 692 PF00069 0.322
MOD_Plk_2-3 299 305 PF00069 0.563
MOD_Plk_2-3 441 447 PF00069 0.348
MOD_Plk_4 15 21 PF00069 0.571
MOD_Plk_4 169 175 PF00069 0.418
MOD_Plk_4 206 212 PF00069 0.494
MOD_Plk_4 256 262 PF00069 0.389
MOD_Plk_4 270 276 PF00069 0.387
MOD_Plk_4 330 336 PF00069 0.571
MOD_Plk_4 421 427 PF00069 0.529
MOD_Plk_4 46 52 PF00069 0.272
MOD_Plk_4 545 551 PF00069 0.382
MOD_Plk_4 66 72 PF00069 0.442
MOD_Plk_4 686 692 PF00069 0.385
MOD_ProDKin_1 126 132 PF00069 0.491
MOD_ProDKin_1 190 196 PF00069 0.479
MOD_ProDKin_1 324 330 PF00069 0.537
MOD_ProDKin_1 658 664 PF00069 0.430
MOD_ProDKin_1 760 766 PF00069 0.540
MOD_SUMO_rev_2 482 489 PF00179 0.418
MOD_SUMO_rev_2 493 502 PF00179 0.427
MOD_SUMO_rev_2 728 733 PF00179 0.346
TRG_DiLeu_BaEn_2 235 241 PF01217 0.369
TRG_DiLeu_BaEn_2 664 670 PF01217 0.382
TRG_DiLeu_BaLyEn_6 468 473 PF01217 0.346
TRG_DiLeu_BaLyEn_6 475 480 PF01217 0.352
TRG_ENDOCYTIC_2 165 168 PF00928 0.425
TRG_ENDOCYTIC_2 201 204 PF00928 0.449
TRG_ENDOCYTIC_2 208 211 PF00928 0.485
TRG_ENDOCYTIC_2 621 624 PF00928 0.416
TRG_ENDOCYTIC_2 737 740 PF00928 0.471
TRG_ENDOCYTIC_2 766 769 PF00928 0.573
TRG_ER_diArg_1 220 223 PF00400 0.393
TRG_ER_diArg_1 29 31 PF00400 0.668
TRG_ER_diArg_1 320 323 PF00400 0.545
TRG_ER_diArg_1 390 393 PF00400 0.540
TRG_ER_diArg_1 476 478 PF00400 0.362
TRG_ER_diArg_1 610 613 PF00400 0.396
TRG_ER_diArg_1 9 12 PF00400 0.612
TRG_NLS_MonoExtC_3 220 225 PF00514 0.333
TRG_NLS_MonoExtN_4 221 226 PF00514 0.332
TRG_Pf-PMV_PEXEL_1 120 124 PF00026 0.668
TRG_Pf-PMV_PEXEL_1 310 314 PF00026 0.537

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IAD3 Leishmania donovani 44% 81%
A0A3Q8IAF8 Leishmania donovani 48% 82%
A0A3Q8IAK8 Leishmania donovani 48% 81%
A0A3Q8IJ32 Leishmania donovani 51% 95%
A0A3S5H6Y1 Leishmania donovani 51% 83%
A0A3S7WTZ8 Leishmania donovani 71% 77%
A0A3S7WU13 Leishmania donovani 51% 84%
A4H8M5 Leishmania braziliensis 54% 100%
A4H8M6 Leishmania braziliensis 51% 100%
A4H8M7 Leishmania braziliensis 54% 86%
A4H8N1 Leishmania braziliensis 46% 81%
A4HWZ5 Leishmania infantum 51% 84%
A4HWZ6 Leishmania infantum 51% 86%
A4HWZ8 Leishmania infantum 51% 86%
A4HX00 Leishmania infantum 71% 77%
A4HX01 Leishmania infantum 44% 100%
A4HX05 Leishmania infantum 48% 82%
E8NHI9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 48% 84%
E9AGP0 Leishmania infantum 52% 100%
E9AQQ9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 50% 91%
E9AQR0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 47% 80%
E9AQR2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 47% 83%
E9AQR3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 70% 77%
E9AQR4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 45% 80%
Q4QER2 Leishmania major 43% 81%
Q4QER3 Leishmania major 71% 100%
Q4QER4 Leishmania major 50% 100%
Q4QER5 Leishmania major 50% 100%
Q4QER6 Leishmania major 50% 100%
Q4QER7 Leishmania major 48% 100%
Q4QER8 Leishmania major 50% 83%
Q4QER9 Leishmania major 50% 100%
Q4QES0 Leishmania major 50% 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