GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Haloechinothrix alba DSM 45207

Align succinyldiaminopimelate transaminase (EC 2.6.1.17); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_089300263.1 CHB84_RS04855 succinyldiaminopimelate transaminase

Query= BRENDA::Q82IK5
         (364 letters)



>NCBI__GCF_900188115.1:WP_089300263.1
          Length = 373

 Score =  431 bits (1108), Expect = e-125
 Identities = 212/357 (59%), Positives = 257/357 (71%)

Query: 8   LPTFPWDKLEPYKARAAAHPDGIVDLSVGTPVDPVPELIQKALVAAADSPGYPTVWGTPE 67
           LP FPWD + PY+A A AHPDG+VDLSVGTPVDPVPE ++ AL A ADSPGYP   GT E
Sbjct: 16  LPDFPWDSIAPYQATARAHPDGVVDLSVGTPVDPVPERVRAALSAKADSPGYPATHGTAE 75

Query: 68  LRDALTGWVERRLGARGVTHHHVLPIVGSKELVAWLPTQLGLGPGDKVAHPRLAYPTYEV 127
           LR  +   +ERR G  GV    VLP +GSKE+VAWLP  LG GPGD V  P LAYPTY+V
Sbjct: 76  LRAEVVAALERRHGVTGVDAEAVLPTIGSKEMVAWLPRLLGFGPGDLVVIPDLAYPTYDV 135

Query: 128 GARLARADHVVYDDPTELDPTGLKLLWLNSPSNPTGKVLSKAELTRIVAWAREHGILVFS 187
           GARLA A     D    + P    ++W+NSPSNPTG++L    L +++ WARE G +V S
Sbjct: 136 GARLAGATVARSDGLVSVGPARPGMMWVNSPSNPTGRILGVDHLRKVLDWARERGTIVVS 195

Query: 188 DECYLELGWEADPVSVLHPDVCGGSYEGIVSVHSLSKRSNLAGYRAAFLAGDPAVLGPLL 247
           DECYL LGW+ +PVSVLHP+V GG  EG++++HSLSK +N+AGYRA F+AGDPA++  LL
Sbjct: 196 DECYLPLGWQDEPVSVLHPEVHGGDLEGVLALHSLSKAANMAGYRAGFVAGDPALVSELL 255

Query: 248 QIRKHGGMMTSAPTQAAVVAALGDDAHVREQRERYAARRTALRDALLSHGFRIEHSEASL 307
            +RKH GM+   P Q A+ AAL DD  +  QR+RYA+RR  LR AL + GFRI+HSEA L
Sbjct: 256 AVRKHAGMIVPRPVQEAMRAALADDEALALQRQRYASRRATLRTALEAAGFRIDHSEAGL 315

Query: 308 YLWATRGESCWDTVAHLADLGILVAPGDFYGSAGEQFVRVALTATDERVAAAVRRLA 364
           YLW +R E  W T+   A+ GILVAPG FYG AG++ VRVALTATDERV AA  RLA
Sbjct: 316 YLWVSRDEDAWQTLEWFAERGILVAPGSFYGPAGQRHVRVALTATDERVTAAAGRLA 372


Lambda     K      H
   0.319    0.135    0.420 

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: 544
Number of extensions: 18
Number of successful extensions: 1
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: 364
Length of database: 373
Length adjustment: 30
Effective length of query: 334
Effective length of database: 343
Effective search space:   114562
Effective search space used:   114562
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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