GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapX in Dyella japonica UNC79MFTsu3.2

Align Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized)
to candidate N515DRAFT_1410 N515DRAFT_1410 methionine aminotransferase

Query= SwissProt::P16524
         (393 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1410
          Length = 381

 Score =  171 bits (433), Expect = 3e-47
 Identities = 113/364 (31%), Positives = 185/364 (50%), Gaps = 13/364 (3%)

Query: 21  SNLVAQHEDVISLTIGQPDFFTPHHVKAAAKKAIDENVTSYTPNAGYLELRQAVQLYMKK 80
           S L  +H+  ++L  G PDF  P  ++ A  +A+ E    Y P  G   LR+ + L  ++
Sbjct: 19  SQLAVEHQ-AVNLGQGFPDFEPPQALREAIARAMAEGRNQYAPGIGLPTLREQIALKTER 77

Query: 81  KADFNYDAESEIIITTGASQAIDAAFRTILSPGDEVIMPGPIYPGYEPIINLCGAKPVIV 140
                 DA  E+ +T+GA++A+ AA   ++  GDEVI+  P Y  YEP+I L GAK V +
Sbjct: 78  MYGRRIDAAGEVTVTSGATEALFAAIAAVVRAGDEVIVFDPAYDSYEPVIELQGAKAVHI 137

Query: 141 DTTSHGFKLTARLIEDALTPNTKCVVLPYPSNPTGVTLSEEELKSIAALLKGRNVFVLSD 200
             T   F +  + + DA+TP T+ +++  P NP+G  LS  +L  +AA+++   + VLSD
Sbjct: 138 PLTVPSFGVDWQRVRDAVTPRTRMILINSPHNPSGAVLSAADLDQLAAIVRDTEIVVLSD 197

Query: 201 EIYSELTYDRP-HYSIATY--LRDQTIVINGLSKSHSMTGWRIGFLFAPKDIAKHILKVH 257
           E+Y  + +D   H S+  +  L  ++IV++   K++  TGW++G+  AP  ++    KVH
Sbjct: 198 EVYEHIVFDGALHQSVLRHAELAARSIVVSSFGKTYHCTGWKLGYAVAPAALSAEFRKVH 257

Query: 258 QYNVSCASSISQKAALEAVTNGFDDALIMREQYKKRLDYVYDRLVSMG----LDVVKPSG 313
           QY   C    +Q A  E + +  +  L +   Y+ + D  +  L++      LDV  P G
Sbjct: 258 QYLTFCTFHPAQVAFAEFMASTPEHYLELPAFYQAKRDR-FRALIAPSRFKLLDV--PGG 314

Query: 314 AFYIFPSIKSFGMTSFDFSMALLEDAGVALVPGSSF--STYGEGYVRLSFACSMDTLREG 371
            F +             F   L++  GVA +P + F  +      VRL FA S  T+   
Sbjct: 315 YFQLVDYSAIRDEPDVTFCEWLVKQGGVAAIPLAPFYETAPDTRLVRLCFAKSDATMDAA 374

Query: 372 LDRL 375
            +RL
Sbjct: 375 AERL 378


Lambda     K      H
   0.319    0.135    0.388 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 305
Number of extensions: 12
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 393
Length of database: 381
Length adjustment: 30
Effective length of query: 363
Effective length of database: 351
Effective search space:   127413
Effective search space used:   127413
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory