LeishMANIAdb
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PHD-type domain-containing protein

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

Quick info

Protein:
PHD-type domain-containing protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania mexicana
UniProt:
E9AZF2_LEIMU
TriTrypDb:
LmxM.27.2430
Length:
570

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

Expansion

Sequence features

E9AZF2
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AZF2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_NRD_NRD_1 147 149 PF00675 0.618
CLV_NRD_NRD_1 186 188 PF00675 0.736
CLV_NRD_NRD_1 206 208 PF00675 0.419
CLV_NRD_NRD_1 403 405 PF00675 0.789
CLV_NRD_NRD_1 555 557 PF00675 0.847
CLV_NRD_NRD_1 60 62 PF00675 0.693
CLV_PCSK_KEX2_1 146 148 PF00082 0.613
CLV_PCSK_KEX2_1 186 188 PF00082 0.736
CLV_PCSK_KEX2_1 206 208 PF00082 0.419
CLV_PCSK_KEX2_1 379 381 PF00082 0.759
CLV_PCSK_KEX2_1 555 557 PF00082 0.847
CLV_PCSK_KEX2_1 60 62 PF00082 0.693
CLV_PCSK_PC1ET2_1 379 381 PF00082 0.759
CLV_PCSK_SKI1_1 355 359 PF00082 0.789
CLV_PCSK_SKI1_1 95 99 PF00082 0.688
DEG_SIAH_1 318 326 PF03145 0.759
DEG_SPOP_SBC_1 560 564 PF00917 0.835
DOC_CKS1_1 192 197 PF01111 0.572
DOC_CKS1_1 463 468 PF01111 0.736
DOC_CYCLIN_yClb3_PxF_3 507 513 PF00134 0.711
DOC_PP2B_LxvP_1 506 509 PF13499 0.725
DOC_PP4_FxxP_1 535 538 PF00568 0.659
DOC_USP7_MATH_1 109 113 PF00917 0.736
DOC_USP7_MATH_1 257 261 PF00917 0.796
DOC_USP7_MATH_1 280 284 PF00917 0.764
DOC_USP7_MATH_1 313 317 PF00917 0.750
DOC_USP7_MATH_1 326 330 PF00917 0.621
DOC_USP7_MATH_1 426 430 PF00917 0.859
DOC_USP7_MATH_1 497 501 PF00917 0.843
DOC_USP7_MATH_1 5 9 PF00917 0.574
DOC_USP7_MATH_1 72 76 PF00917 0.643
DOC_WW_Pin1_4 123 128 PF00397 0.731
DOC_WW_Pin1_4 178 183 PF00397 0.729
DOC_WW_Pin1_4 191 196 PF00397 0.450
DOC_WW_Pin1_4 248 253 PF00397 0.646
DOC_WW_Pin1_4 315 320 PF00397 0.826
DOC_WW_Pin1_4 321 326 PF00397 0.735
DOC_WW_Pin1_4 327 332 PF00397 0.636
DOC_WW_Pin1_4 407 412 PF00397 0.832
DOC_WW_Pin1_4 418 423 PF00397 0.674
DOC_WW_Pin1_4 439 444 PF00397 0.836
DOC_WW_Pin1_4 448 453 PF00397 0.705
DOC_WW_Pin1_4 456 461 PF00397 0.576
DOC_WW_Pin1_4 462 467 PF00397 0.596
DOC_WW_Pin1_4 484 489 PF00397 0.699
LIG_14-3-3_CanoR_1 25 29 PF00244 0.610
LIG_14-3-3_CanoR_1 343 349 PF00244 0.833
LIG_14-3-3_CanoR_1 434 443 PF00244 0.636
LIG_14-3-3_CanoR_1 54 62 PF00244 0.687
LIG_14-3-3_CanoR_1 68 76 PF00244 0.532
LIG_BIR_II_1 1 5 PF00653 0.629
LIG_EVH1_1 506 510 PF00568 0.723
LIG_EVH1_2 509 513 PF00568 0.793
LIG_FHA_1 47 53 PF00498 0.669
LIG_FHA_1 96 102 PF00498 0.670
LIG_FHA_2 137 143 PF00498 0.663
LIG_FHA_2 32 38 PF00498 0.667
LIG_FHA_2 384 390 PF00498 0.766
LIG_FHA_2 561 567 PF00498 0.830
LIG_LIR_Apic_2 478 484 PF02991 0.612
LIG_LIR_Gen_1 151 160 PF02991 0.600
LIG_LIR_Gen_1 19 28 PF02991 0.669
LIG_LIR_Nem_3 19 24 PF02991 0.661
LIG_PROFILIN_1 466 472 PF00235 0.729
LIG_PROFILIN_1 488 494 PF00235 0.700
LIG_PTAP_UEV_1 242 247 PF05743 0.702
LIG_RPA_C_Fungi 369 381 PF08784 0.644
LIG_SH2_CRK 481 485 PF00017 0.744
LIG_SH2_NCK_1 481 485 PF00017 0.744
LIG_SH2_SRC 481 484 PF00017 0.645
LIG_SH2_STAP1 199 203 PF00017 0.672
LIG_SH2_STAT5 152 155 PF00017 0.673
LIG_SH3_1 449 455 PF00018 0.672
LIG_SH3_2 243 248 PF14604 0.700
LIG_SH3_2 341 346 PF14604 0.623
LIG_SH3_2 551 556 PF14604 0.842
LIG_SH3_3 162 168 PF00018 0.733
LIG_SH3_3 240 246 PF00018 0.763
LIG_SH3_3 258 264 PF00018 0.560
LIG_SH3_3 282 288 PF00018 0.586
LIG_SH3_3 338 344 PF00018 0.568
LIG_SH3_3 406 412 PF00018 0.748
LIG_SH3_3 440 446 PF00018 0.616
LIG_SH3_3 449 455 PF00018 0.736
LIG_SH3_3 457 463 PF00018 0.654
LIG_SH3_3 464 470 PF00018 0.653
LIG_SH3_3 482 488 PF00018 0.547
LIG_SH3_3 489 495 PF00018 0.686
LIG_SH3_3 504 510 PF00018 0.584
LIG_SH3_3 548 554 PF00018 0.655
LIG_TRAF2_1 112 115 PF00917 0.700
LIG_WW_3 421 425 PF00397 0.816
MOD_CDC14_SPxK_1 421 424 PF00782 0.775
MOD_CDK_SPxK_1 418 424 PF00069 0.816
MOD_CDK_SPxxK_3 321 328 PF00069 0.765
MOD_CDK_SPxxK_3 442 449 PF00069 0.625
MOD_CK1_1 121 127 PF00069 0.808
MOD_CK1_1 134 140 PF00069 0.562
MOD_CK1_1 251 257 PF00069 0.712
MOD_CK1_1 3 9 PF00069 0.640
MOD_CK1_1 307 313 PF00069 0.837
MOD_CK1_1 315 321 PF00069 0.684
MOD_CK1_1 360 366 PF00069 0.832
MOD_CK1_1 369 375 PF00069 0.692
MOD_CK1_1 384 390 PF00069 0.604
MOD_CK1_1 393 399 PF00069 0.691
MOD_CK1_1 427 433 PF00069 0.754
MOD_CK1_1 437 443 PF00069 0.690
MOD_CK1_1 454 460 PF00069 0.558
MOD_CK1_1 475 481 PF00069 0.554
MOD_CK1_1 55 61 PF00069 0.687
MOD_CK1_1 562 568 PF00069 0.827
MOD_CK2_1 109 115 PF00069 0.742
MOD_CK2_1 136 142 PF00069 0.676
MOD_CK2_1 156 162 PF00069 0.595
MOD_CK2_1 31 37 PF00069 0.540
MOD_GlcNHglycan 230 233 PF01048 0.585
MOD_GlcNHglycan 243 246 PF01048 0.781
MOD_GlcNHglycan 253 256 PF01048 0.673
MOD_GlcNHglycan 311 314 PF01048 0.723
MOD_GlcNHglycan 315 318 PF01048 0.747
MOD_GlcNHglycan 319 322 PF01048 0.691
MOD_GlcNHglycan 34 37 PF01048 0.552
MOD_GlcNHglycan 346 349 PF01048 0.830
MOD_GlcNHglycan 371 374 PF01048 0.843
MOD_GlcNHglycan 399 402 PF01048 0.609
MOD_GlcNHglycan 426 429 PF01048 0.821
MOD_GlcNHglycan 436 439 PF01048 0.724
MOD_GlcNHglycan 474 477 PF01048 0.769
MOD_GlcNHglycan 499 502 PF01048 0.770
MOD_GlcNHglycan 535 538 PF01048 0.606
MOD_GlcNHglycan 539 542 PF01048 0.750
MOD_GlcNHglycan 54 57 PF01048 0.468
MOD_GlcNHglycan 7 10 PF01048 0.520
MOD_GSK3_1 117 124 PF00069 0.740
MOD_GSK3_1 130 137 PF00069 0.588
MOD_GSK3_1 237 244 PF00069 0.771
MOD_GSK3_1 304 311 PF00069 0.733
MOD_GSK3_1 313 320 PF00069 0.678
MOD_GSK3_1 327 334 PF00069 0.589
MOD_GSK3_1 357 364 PF00069 0.832
MOD_GSK3_1 381 388 PF00069 0.763
MOD_GSK3_1 389 396 PF00069 0.712
MOD_GSK3_1 426 433 PF00069 0.815
MOD_GSK3_1 471 478 PF00069 0.545
MOD_GSK3_1 533 540 PF00069 0.780
MOD_GSK3_1 63 70 PF00069 0.551
MOD_N-GLC_1 257 262 PF02516 0.542
MOD_NEK2_1 131 136 PF00069 0.728
MOD_NEK2_1 24 29 PF00069 0.572
MOD_NEK2_1 305 310 PF00069 0.834
MOD_NEK2_1 333 338 PF00069 0.568
MOD_NEK2_1 357 362 PF00069 0.832
MOD_NEK2_1 415 420 PF00069 0.800
MOD_NEK2_1 514 519 PF00069 0.839
MOD_PIKK_1 63 69 PF00454 0.677
MOD_PIKK_1 84 90 PF00454 0.649
MOD_PKA_2 24 30 PF00069 0.606
MOD_PKA_2 430 436 PF00069 0.631
MOD_PKA_2 67 73 PF00069 0.667
MOD_Plk_1 257 263 PF00069 0.538
MOD_Plk_1 3 9 PF00069 0.635
MOD_Plk_2-3 110 116 PF00069 0.553
MOD_ProDKin_1 123 129 PF00069 0.731
MOD_ProDKin_1 178 184 PF00069 0.728
MOD_ProDKin_1 191 197 PF00069 0.441
MOD_ProDKin_1 248 254 PF00069 0.650
MOD_ProDKin_1 315 321 PF00069 0.829
MOD_ProDKin_1 327 333 PF00069 0.637
MOD_ProDKin_1 407 413 PF00069 0.831
MOD_ProDKin_1 418 424 PF00069 0.677
MOD_ProDKin_1 439 445 PF00069 0.837
MOD_ProDKin_1 448 454 PF00069 0.708
MOD_ProDKin_1 456 462 PF00069 0.571
MOD_ProDKin_1 484 490 PF00069 0.697
MOD_SUMO_for_1 297 300 PF00179 0.742
TRG_DiLeu_BaEn_4 12 18 PF01217 0.712
TRG_ENDOCYTIC_2 152 155 PF00928 0.595
TRG_ER_diArg_1 145 148 PF00400 0.614
TRG_ER_diArg_1 186 188 PF00400 0.736
TRG_ER_diArg_1 217 220 PF00400 0.544
TRG_ER_diArg_1 554 556 PF00400 0.840
TRG_ER_diArg_1 60 62 PF00400 0.693
TRG_Pf-PMV_PEXEL_1 220 224 PF00026 0.547

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3S7X110 Leishmania donovani 87% 100%
A4HG23 Leishmania braziliensis 72% 100%
A4I344 Leishmania infantum 87% 100%
E9ACW3 Leishmania major 87% 100%

Download

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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