GapMind for Amino acid biosynthesis

 

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

Align [LysW]-aminoadipate semialdehyde/glutamate semialdehyde transaminase; EC 2.6.1.118; EC 2.6.1.124 (uncharacterized)
to candidate WP_007473232.1 CMTB2_RS01220 glutamate-1-semialdehyde-2,1-aminomutase

Query= curated2:Q7SI94
         (388 letters)



>NCBI__GCF_000170735.1:WP_007473232.1
          Length = 420

 Score =  145 bits (366), Expect = 2e-39
 Identities = 109/319 (34%), Positives = 161/319 (50%), Gaps = 31/319 (9%)

Query: 15  IIKGEGQYVWDEKNNKYLDMHAGHGVAFLGHRNK----VIIDHLKKQMEEISTLSLAFDT 70
           I KGEG Y++D + NKYLD     G    GH +K     II+ +KK +      S    T
Sbjct: 32  IEKGEGAYIFDIEGNKYLDYIQSWGPLIFGHCDKDTQNAIIEAVKKGV------SFGAPT 85

Query: 71  PIREEMIKELDELKPEDLDNLFLLNSGSEAVELALKIARKITKRRKIVAFKNSFHGRSMG 130
            +  E+ KE+ EL P  L+ +  +NSG+EA   A+++AR  T +  I+ F+  +HG S  
Sbjct: 86  KVEVELAKEVLELFPH-LNLIRFVNSGTEATMSAIRLARGYTGKDDIIKFEGCYHGHSDS 144

Query: 131 ALSVTWN--KKYREPFEPLIGPVEFLE------YNNVDSLKSITE--DTAAVIVEPVQGE 180
            L    +    +  P  P + P +F +      YN+++S+K   E  D   VI+EP+ G 
Sbjct: 145 LLVSAGSGAATFGVPSSPGV-PADFTKHTLLAKYNDIESVKKCFENGDVGCVIIEPIAGN 203

Query: 181 GGVIPAKKEFVKSLREVTEKVNALLIIDEVQTGFGRTGKIWAYQHFDIKPDILTAGKAIG 240
             ++P +KEF+  LRE+     A+LI DEV +GF R     ++  + IK DI+T GK IG
Sbjct: 204 MSLVPGEKEFLGELREICNHYGAVLIFDEVMSGF-RASLRGSFDIYGIKADIVTFGKVIG 262

Query: 241 GGFPVSAVFLPNWISEKIEEGD---HGSTYGGNPLAAAAVTAACKVAKS-----EKIAEQ 292
           GG PV A      I EK+          T  GNP+A +A     K  K      +++ ++
Sbjct: 263 GGMPVGAFAGKKEIMEKLSPVGPVYQAGTLSGNPVAMSAGLTVIKKLKENPEIYKELEDK 322

Query: 293 AQKKGELFMRILKEKLEDF 311
           A+K  E F  I KE   DF
Sbjct: 323 AKKLMEGFSEISKENNIDF 341


Lambda     K      H
   0.317    0.136    0.386 

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: 398
Number of extensions: 19
Number of successful extensions: 4
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: 420
Length adjustment: 31
Effective length of query: 357
Effective length of database: 389
Effective search space:   138873
Effective search space used:   138873
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 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