GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysY in Thermithiobacillus tepidarius DSM 3134

Align Putative [LysW]-L-2-aminoadipate/[LysW]-L-glutamate phosphate reductase; EC 1.2.1.103; EC 1.2.1.106 (uncharacterized)
to candidate WP_028990530.1 G579_RS0113080 N-acetyl-gamma-glutamyl-phosphate reductase

Query= curated2:A0RWW0
         (348 letters)



>NCBI__GCF_000423825.1:WP_028990530.1
          Length = 346

 Score =  261 bits (667), Expect = 2e-74
 Identities = 145/349 (41%), Positives = 202/349 (57%), Gaps = 7/349 (2%)

Query: 1   MKVGVVGASGYVGGETLRLLVNHPDVEIAAVTSRQHVGEYLHRVQPSLRGFTDLTFSELD 60
           ++VG+VG +GY G E LRLL  HP   + A+TSR   G  +  + P+LRG  +L+FSE D
Sbjct: 3   IRVGIVGGTGYTGVELLRLLARHPGARVTAITSRAEAGMRVDALFPNLRGHCELSFSEPD 62

Query: 61  YDRLSDSCDLVFTAVPHGTATDIVRALYDRDIKVIDLSADYRLHDPADYTKWYGWEHPHP 120
              L+ +CD+VF A PHG A D+   L    +KVIDL AD+RL DPA + +WYG EH   
Sbjct: 63  PAALAATCDVVFFATPHGVAMDLAPQLLAAGVKVIDLGADFRLRDPATFARWYGMEHRAL 122

Query: 121 DYLSKSVFGIPELHREEIRSAKLVSCPGCMAVTSILALAPPVREGLVDTEHIVVDSKIGS 180
           D+L K+V+G+PE  R  IR A+L++ PGC    + L   P +  GL+D   ++ D+K G+
Sbjct: 123 DWLEKAVYGLPETRRAAIREAQLIANPGCYPTATQLGFLPLLEAGLLDPHSLIADTKSGA 182

Query: 181 SGAGAGAGTAHAM-RAG-VIRPYKPAKHRHTGEIEQELSGIAGKKIRVSMSPHAVDVVRG 238
           SGAG  A   + +  AG     Y  + HRH  EIEQELS  AG ++RV+  PH   ++RG
Sbjct: 183 SGAGRAAKLPNLLCEAGDSFSAYAVSGHRHQPEIEQELSCWAGGEVRVTFVPHLTPMIRG 242

Query: 239 ILCTNHVFLTREASEKDLWKMYRQAYGEERFVRLIRDKKGLYKFPDPKFLVGSNFCDIGF 298
           I  T +  LTR+    DL  +Y   Y EE FV ++         P  + + G+N C I  
Sbjct: 243 IHATLYGRLTRDIDAADLQVLYEARYREEPFVDVLPPG----SHPATRSVRGANVCRIAV 298

Query: 299 DLDEDNNRLVAISASDNLMKGAAGSAIQNMNIMAGLDEMSGLRYTPLTP 347
                  ++V +S  DNL+KGA+G A+QNMN++ GL E  GL    L P
Sbjct: 299 HQPRP-GQVVVLSVIDNLVKGASGQAVQNMNLLFGLPEAMGLEDVALMP 346


Lambda     K      H
   0.320    0.137    0.412 

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: 298
Number of extensions: 17
Number of successful extensions: 3
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: 348
Length of database: 346
Length adjustment: 29
Effective length of query: 319
Effective length of database: 317
Effective search space:   101123
Effective search space used:   101123
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: 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