LeishMANIAdb
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AP2 domain transcription factor AP2X-11

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

Quick info

Protein:
AP2 domain transcription factor AP2X-11
Gene product:
hypothetical protein, unknown function
Species:
Leishmania braziliensis
UniProt:
A4HJQ4_LEIBR
TriTrypDb:
LbrM.31.3000 , LBRM2903_310039300 *
Length:
590

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 yes yes: 1, no: 4
NetGPI no yes: 0, no: 5
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

A4HJQ4
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HJQ4

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 273 277 PF00656 0.574
CLV_NRD_NRD_1 459 461 PF00675 0.831
CLV_NRD_NRD_1 463 465 PF00675 0.759
CLV_NRD_NRD_1 497 499 PF00675 0.643
CLV_PCSK_FUR_1 495 499 PF00082 0.604
CLV_PCSK_KEX2_1 459 461 PF00082 0.831
CLV_PCSK_KEX2_1 463 465 PF00082 0.759
CLV_PCSK_KEX2_1 497 499 PF00082 0.643
CLV_PCSK_KEX2_1 79 81 PF00082 0.563
CLV_PCSK_PC1ET2_1 79 81 PF00082 0.563
CLV_PCSK_PC7_1 459 465 PF00082 0.827
CLV_PCSK_SKI1_1 275 279 PF00082 0.687
CLV_PCSK_SKI1_1 423 427 PF00082 0.629
DOC_AGCK_PIF_1 149 154 PF00069 0.576
DOC_CKS1_1 439 444 PF01111 0.702
DOC_MAPK_MEF2A_6 355 364 PF00069 0.599
DOC_PP2B_LxvP_1 118 121 PF13499 0.595
DOC_PP4_FxxP_1 211 214 PF00568 0.536
DOC_PP4_FxxP_1 439 442 PF00568 0.546
DOC_USP7_MATH_1 171 175 PF00917 0.791
DOC_USP7_MATH_1 181 185 PF00917 0.545
DOC_USP7_MATH_1 247 251 PF00917 0.574
DOC_USP7_MATH_1 262 266 PF00917 0.510
DOC_USP7_MATH_1 301 305 PF00917 0.682
DOC_USP7_MATH_1 348 352 PF00917 0.787
DOC_USP7_MATH_1 413 417 PF00917 0.522
DOC_USP7_MATH_1 431 435 PF00917 0.802
DOC_USP7_MATH_1 488 492 PF00917 0.686
DOC_USP7_MATH_1 555 559 PF00917 0.549
DOC_USP7_MATH_1 560 564 PF00917 0.542
DOC_USP7_MATH_1 58 62 PF00917 0.736
DOC_USP7_MATH_1 63 67 PF00917 0.693
DOC_USP7_UBL2_3 338 342 PF12436 0.829
DOC_WW_Pin1_4 177 182 PF00397 0.706
DOC_WW_Pin1_4 297 302 PF00397 0.713
DOC_WW_Pin1_4 32 37 PF00397 0.531
DOC_WW_Pin1_4 354 359 PF00397 0.671
DOC_WW_Pin1_4 379 384 PF00397 0.571
DOC_WW_Pin1_4 438 443 PF00397 0.602
DOC_WW_Pin1_4 445 450 PF00397 0.615
DOC_WW_Pin1_4 452 457 PF00397 0.611
DOC_WW_Pin1_4 564 569 PF00397 0.578
DOC_WW_Pin1_4 64 69 PF00397 0.568
DOC_WW_Pin1_4 88 93 PF00397 0.812
LIG_14-3-3_CanoR_1 124 132 PF00244 0.637
LIG_14-3-3_CanoR_1 241 247 PF00244 0.686
LIG_14-3-3_CanoR_1 264 268 PF00244 0.573
LIG_14-3-3_CanoR_1 392 396 PF00244 0.499
LIG_14-3-3_CanoR_1 417 423 PF00244 0.748
LIG_14-3-3_CanoR_1 463 473 PF00244 0.773
LIG_14-3-3_CanoR_1 477 485 PF00244 0.631
LIG_14-3-3_CanoR_1 549 557 PF00244 0.673
LIG_14-3-3_CanoR_1 574 578 PF00244 0.601
LIG_Actin_WH2_2 537 554 PF00022 0.542
LIG_APCC_ABBAyCdc20_2 107 113 PF00400 0.546
LIG_BRCT_BRCA1_1 107 111 PF00533 0.544
LIG_BRCT_BRCA1_1 265 269 PF00533 0.818
LIG_BRCT_BRCA1_1 392 396 PF00533 0.713
LIG_BRCT_BRCA1_1 468 472 PF00533 0.554
LIG_BRCT_BRCA1_1 8 12 PF00533 0.491
LIG_EH_1 176 180 PF12763 0.582
LIG_FHA_1 23 29 PF00498 0.526
LIG_FHA_1 479 485 PF00498 0.573
LIG_FHA_1 65 71 PF00498 0.567
LIG_FHA_2 567 573 PF00498 0.691
LIG_LIR_Apic_2 208 214 PF02991 0.531
LIG_LIR_Gen_1 146 154 PF02991 0.582
LIG_LIR_Gen_1 359 368 PF02991 0.690
LIG_LIR_Gen_1 376 386 PF02991 0.464
LIG_LIR_Gen_1 479 488 PF02991 0.576
LIG_LIR_Gen_1 512 520 PF02991 0.529
LIG_LIR_Gen_1 7 16 PF02991 0.494
LIG_LIR_Nem_3 146 152 PF02991 0.582
LIG_LIR_Nem_3 359 364 PF02991 0.782
LIG_LIR_Nem_3 376 381 PF02991 0.513
LIG_LIR_Nem_3 440 446 PF02991 0.566
LIG_LIR_Nem_3 479 483 PF02991 0.572
LIG_LIR_Nem_3 512 518 PF02991 0.527
LIG_LIR_Nem_3 7 11 PF02991 0.490
LIG_MYND_1 117 121 PF01753 0.587
LIG_Pex14_2 8 12 PF04695 0.491
LIG_SH2_STAT5 443 446 PF00017 0.547
LIG_SH3_3 14 20 PF00018 0.496
LIG_SH3_3 175 181 PF00018 0.618
LIG_SH3_3 304 310 PF00018 0.589
LIG_SH3_3 482 488 PF00018 0.795
LIG_SH3_3 65 71 PF00018 0.820
LIG_SH3_3 79 85 PF00018 0.600
LIG_SxIP_EBH_1 254 268 PF03271 0.564
LIG_TRAF2_1 363 366 PF00917 0.587
MOD_CDC14_SPxK_1 91 94 PF00782 0.549
MOD_CDK_SPK_2 64 69 PF00069 0.568
MOD_CDK_SPxK_1 564 570 PF00069 0.580
MOD_CDK_SPxK_1 88 94 PF00069 0.559
MOD_CDK_SPxxK_3 452 459 PF00069 0.558
MOD_CDK_SPxxK_3 88 95 PF00069 0.557
MOD_CK1_1 145 151 PF00069 0.708
MOD_CK1_1 170 176 PF00069 0.797
MOD_CK1_1 192 198 PF00069 0.537
MOD_CK1_1 242 248 PF00069 0.659
MOD_CK1_1 250 256 PF00069 0.700
MOD_CK1_1 346 352 PF00069 0.726
MOD_CK1_1 354 360 PF00069 0.793
MOD_CK1_1 369 375 PF00069 0.578
MOD_CK1_1 387 393 PF00069 0.481
MOD_CK1_1 416 422 PF00069 0.767
MOD_CK1_1 479 485 PF00069 0.573
MOD_CK1_1 489 495 PF00069 0.550
MOD_CK1_1 531 537 PF00069 0.800
MOD_CK1_1 576 582 PF00069 0.796
MOD_CK1_1 61 67 PF00069 0.565
MOD_CK2_1 319 325 PF00069 0.596
MOD_CK2_1 360 366 PF00069 0.585
MOD_CK2_1 464 470 PF00069 0.556
MOD_CK2_1 501 507 PF00069 0.660
MOD_CK2_1 539 545 PF00069 0.567
MOD_CK2_1 566 572 PF00069 0.661
MOD_Cter_Amidation 77 80 PF01082 0.558
MOD_GlcNHglycan 112 116 PF01048 0.582
MOD_GlcNHglycan 135 138 PF01048 0.788
MOD_GlcNHglycan 169 172 PF01048 0.825
MOD_GlcNHglycan 253 256 PF01048 0.645
MOD_GlcNHglycan 330 334 PF01048 0.600
MOD_GlcNHglycan 368 371 PF01048 0.622
MOD_GlcNHglycan 389 392 PF01048 0.754
MOD_GlcNHglycan 429 432 PF01048 0.797
MOD_GlcNHglycan 433 436 PF01048 0.732
MOD_GlcNHglycan 488 491 PF01048 0.673
MOD_GlcNHglycan 584 587 PF01048 0.765
MOD_GlcNHglycan 63 66 PF01048 0.690
MOD_GSK3_1 101 108 PF00069 0.794
MOD_GSK3_1 119 126 PF00069 0.542
MOD_GSK3_1 143 150 PF00069 0.707
MOD_GSK3_1 155 162 PF00069 0.701
MOD_GSK3_1 166 173 PF00069 0.655
MOD_GSK3_1 177 184 PF00069 0.565
MOD_GSK3_1 18 25 PF00069 0.496
MOD_GSK3_1 188 195 PF00069 0.583
MOD_GSK3_1 203 210 PF00069 0.588
MOD_GSK3_1 242 249 PF00069 0.607
MOD_GSK3_1 251 258 PF00069 0.682
MOD_GSK3_1 281 288 PF00069 0.832
MOD_GSK3_1 297 304 PF00069 0.699
MOD_GSK3_1 356 363 PF00069 0.641
MOD_GSK3_1 387 394 PF00069 0.555
MOD_GSK3_1 412 419 PF00069 0.653
MOD_GSK3_1 427 434 PF00069 0.790
MOD_GSK3_1 520 527 PF00069 0.659
MOD_GSK3_1 560 567 PF00069 0.674
MOD_GSK3_1 573 580 PF00069 0.738
MOD_GSK3_1 59 66 PF00069 0.605
MOD_N-GLC_1 165 170 PF02516 0.771
MOD_N-GLC_1 239 244 PF02516 0.582
MOD_N-GLC_1 387 392 PF02516 0.519
MOD_N-GLC_1 431 436 PF02516 0.800
MOD_NEK2_1 105 110 PF00069 0.809
MOD_NEK2_1 111 116 PF00069 0.738
MOD_NEK2_1 165 170 PF00069 0.651
MOD_NEK2_1 189 194 PF00069 0.666
MOD_NEK2_1 239 244 PF00069 0.612
MOD_NEK2_1 251 256 PF00069 0.548
MOD_NEK2_1 343 348 PF00069 0.579
MOD_NEK2_1 384 389 PF00069 0.516
MOD_NEK2_1 577 582 PF00069 0.836
MOD_NEK2_2 263 268 PF00069 0.567
MOD_NEK2_2 391 396 PF00069 0.503
MOD_NEK2_2 41 46 PF00069 0.564
MOD_NEK2_2 560 565 PF00069 0.565
MOD_PIKK_1 416 422 PF00454 0.607
MOD_PIKK_1 489 495 PF00454 0.589
MOD_PK_1 34 40 PF00069 0.532
MOD_PKA_1 459 465 PF00069 0.827
MOD_PKA_2 123 129 PF00069 0.710
MOD_PKA_2 263 269 PF00069 0.691
MOD_PKA_2 391 397 PF00069 0.498
MOD_PKA_2 416 422 PF00069 0.767
MOD_PKA_2 427 433 PF00069 0.475
MOD_PKA_2 459 465 PF00069 0.827
MOD_PKA_2 476 482 PF00069 0.537
MOD_PKA_2 524 530 PF00069 0.686
MOD_PKA_2 531 537 PF00069 0.612
MOD_PKA_2 555 561 PF00069 0.601
MOD_PKA_2 573 579 PF00069 0.526
MOD_Plk_1 189 195 PF00069 0.544
MOD_Plk_1 239 245 PF00069 0.582
MOD_Plk_1 41 47 PF00069 0.562
MOD_Plk_2-3 190 196 PF00069 0.579
MOD_Plk_2-3 281 287 PF00069 0.605
MOD_Plk_2-3 319 325 PF00069 0.596
MOD_Plk_2-3 501 507 PF00069 0.597
MOD_Plk_4 256 262 PF00069 0.651
MOD_Plk_4 319 325 PF00069 0.596
MOD_Plk_4 391 397 PF00069 0.511
MOD_Plk_4 421 427 PF00069 0.772
MOD_Plk_4 479 485 PF00069 0.573
MOD_ProDKin_1 177 183 PF00069 0.708
MOD_ProDKin_1 297 303 PF00069 0.713
MOD_ProDKin_1 32 38 PF00069 0.533
MOD_ProDKin_1 354 360 PF00069 0.673
MOD_ProDKin_1 379 385 PF00069 0.573
MOD_ProDKin_1 438 444 PF00069 0.605
MOD_ProDKin_1 445 451 PF00069 0.614
MOD_ProDKin_1 452 458 PF00069 0.614
MOD_ProDKin_1 564 570 PF00069 0.580
MOD_ProDKin_1 64 70 PF00069 0.569
MOD_ProDKin_1 88 94 PF00069 0.811
MOD_SUMO_for_1 39 42 PF00179 0.547
MOD_SUMO_rev_2 273 280 PF00179 0.821
TRG_DiLeu_BaEn_1 319 324 PF01217 0.595
TRG_DiLeu_BaEn_2 467 473 PF01217 0.555
TRG_DiLeu_BaLyEn_6 114 119 PF01217 0.586
TRG_ENDOCYTIC_2 443 446 PF00928 0.547
TRG_ER_diArg_1 458 460 PF00400 0.834
TRG_ER_diArg_1 495 498 PF00400 0.621
TRG_ER_diArg_1 546 549 PF00400 0.533
TRG_Pf-PMV_PEXEL_1 268 273 PF00026 0.567
TRG_Pf-PMV_PEXEL_1 471 475 PF00026 0.652

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IKC7 Leishmania donovani 53% 100%
A4I770 Leishmania infantum 53% 100%
E9B265 Leishmania mexicana (strain MHOM/GT/2001/U1103) 51% 100%
Q4Q5Z5 Leishmania major 52% 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