GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysN in Caminibacter mediatlanticus TB-2

Align 2-aminoadipate transaminase; 2-aminoadipate aminotransferase; L-2AA aminotransferase; EC 2.6.1.39 (characterized)
to candidate WP_007473232.1 CMTB2_RS01220 glutamate-1-semialdehyde-2,1-aminomutase

Query= SwissProt::Q88FI7
         (416 letters)



>NCBI__GCF_000170735.1:WP_007473232.1
          Length = 420

 Score =  130 bits (326), Expect = 1e-34
 Identities = 96/319 (30%), Positives = 153/319 (47%), Gaps = 36/319 (11%)

Query: 15  PITLSHGRNAEVWDTDGKRYIDFVGGIGVLNLGHCNP----AVVEAIQAQATRLTHYAFN 70
           P  +  G  A ++D +G +Y+D++   G L  GHC+     A++EA++            
Sbjct: 29  PPFIEKGEGAYIFDIEGNKYLDYIQSWGPLIFGHCDKDTQNAIIEAVK-----------K 77

Query: 71  AAPHGPYLALMEQLSQFVPVSYPLAGML--TNSGAEAAENALKVARGATGKRAIIAFDGG 128
               G    +  +L++ V   +P   ++   NSG EA  +A+++ARG TGK  II F+G 
Sbjct: 78  GVSFGAPTKVEVELAKEVLELFPHLNLIRFVNSGTEATMSAIRLARGYTGKDDIIKFEGC 137

Query: 129 FHGRTLATLNLNGKVAPYKQRVGELPGPVYHLP-YPSADTGVTCEQALKAMDRLFSVELA 187
           +HG + + L   G  A             + +P  P      T    L   + + SV+  
Sbjct: 138 YHGHSDSLLVSAGSGA-----------ATFGVPSSPGVPADFTKHTLLAKYNDIESVKKC 186

Query: 188 VE--DVAAFIFEPVQGEGGFLALDPAFAQALRRFCDERGILIIIDEIQSGFGRTGQRFAF 245
            E  DV   I EP+ G    +  +  F   LR  C+  G ++I DE+ SGF R   R +F
Sbjct: 187 FENGDVGCVIIEPIAGNMSLVPGEKEFLGELREICNHYGAVLIFDEVMSGF-RASLRGSF 245

Query: 246 PRLGIEPDLLLLAKSIAGGMPLGAVVGRKELMAALPKGG---LGGTYSGNPISCAAALAS 302
              GI+ D++   K I GGMP+GA  G+KE+M  L   G     GT SGNP++ +A L  
Sbjct: 246 DIYGIKADIVTFGKVIGGGMPVGAFAGKKEIMEKLSPVGPVYQAGTLSGNPVAMSAGLTV 305

Query: 303 LAQMTDENLATWGERQEQA 321
           + ++  EN   + E +++A
Sbjct: 306 IKKL-KENPEIYKELEDKA 323


Lambda     K      H
   0.320    0.137    0.402 

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: 409
Number of extensions: 19
Number of successful extensions: 5
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: 416
Length of database: 420
Length adjustment: 32
Effective length of query: 384
Effective length of database: 388
Effective search space:   148992
Effective search space used:   148992
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 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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