GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Synechococcus elongatus PCC 7942

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate Synpcc7942_2545 Synpcc7942_2545 aspartate aminotransferase

Query= BRENDA::Q8YMS6
         (388 letters)



>FitnessBrowser__SynE:Synpcc7942_2545
          Length = 392

 Score =  540 bits (1390), Expect = e-158
 Identities = 269/386 (69%), Positives = 320/386 (82%)

Query: 1   MKLAARVSQVTPSITLAIAAKAKAMKAEGIDVCSFSAGEPDFDTPAHIKAAAAKALDEGK 60
           MKL+ RV +V+PS+TLAIAA+AKAMKAEG+DVCSFSAGEPDF+TP HI+ AAA+AL EGK
Sbjct: 1   MKLSERVGRVSPSLTLAIAAQAKAMKAEGLDVCSFSAGEPDFETPLHIRNAAAQALAEGK 60

Query: 61  TKYGAAAGEPKLREAIARKLQKDNHLDYKPENVIVTNGGKHSLYNLIVALIDPGDEVIIP 120
           T+YG AAGEP LREAIA+KL+ DN LDY+  N++VTNGGK SLYNL+  L+DPGDEVIIP
Sbjct: 61  TRYGPAAGEPDLREAIAQKLRADNGLDYQAANILVTNGGKQSLYNLMQVLLDPGDEVIIP 120

Query: 121 APYWLSYPEMVTLVGGKSVIVPTDASTGYKITPEQLRKAITPKTKLFVLNSPSNPTGMVY 180
           APYWLSYPEMV L GG  VIV T AS G+K+ P+QL  AITP+T+L VLNSPSNPTGMVY
Sbjct: 121 APYWLSYPEMVKLAGGVPVIVETFASDGFKLQPQQLAGAITPRTRLLVLNSPSNPTGMVY 180

Query: 181 TPEEIKALAQVVVDADIYVVSDEIYEKILYDGAQHISIGSLGKEIFNRTLISNGFAKAYS 240
           + +E++A+A ++   D +VVSDEIYEKILYDGA H SIGSL    F RTLISNGFAKAYS
Sbjct: 181 SRQELEAIAPIIEAHDFWVVSDEIYEKILYDGADHHSIGSLSPACFERTLISNGFAKAYS 240

Query: 241 MTGWRLGYLAGPVDIIKAASSIQGHSTSNVCTFAQYGAIAALEDSQDCVEEMRQAFAKRR 300
           MTGWR+GYLAGP ++I AA+S+Q HSTSNVCTFAQYGAIAAL+  QDCV EM  AF +RR
Sbjct: 241 MTGWRVGYLAGPSELIAAAASLQSHSTSNVCTFAQYGAIAALQGPQDCVAEMLAAFTERR 300

Query: 301 QVMLDRLNAIPGLSTAKPDGAFYLFPDISKTGLKSLEFCDALIEEHKVAVIPGIAFGADD 360
           Q++L+ LN I GLS   P+GAFY+F DISKTGL S+ +C  L+++H+VA IPGIAFG D 
Sbjct: 301 QLILNGLNQIAGLSCPIPEGAFYVFVDISKTGLDSMTYCRQLLDQHQVAAIPGIAFGDDR 360

Query: 361 NIRLSYATDLATIEKGLDRLEKFVRS 386
           +IRLSYATD  TIEKGL+RL+ F  S
Sbjct: 361 SIRLSYATDCQTIEKGLERLQLFQNS 386


Lambda     K      H
   0.317    0.134    0.381 

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: 439
Number of extensions: 10
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: 388
Length of database: 392
Length adjustment: 31
Effective length of query: 357
Effective length of database: 361
Effective search space:   128877
Effective search space used:   128877
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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