GapMind for Amino acid biosynthesis

 

Alignments for a candidate for proA in Herbaspirillum seropedicae SmR1

Align glutamate-5-semialdehyde dehydrogenase (EC 1.2.1.41) (characterized)
to candidate HSERO_RS01815 HSERO_RS01815 gamma-glutamyl kinase

Query= BRENDA::Q941T1
         (735 letters)



>FitnessBrowser__HerbieS:HSERO_RS01815
          Length = 372

 Score =  157 bits (398), Expect = 7e-43
 Identities = 122/373 (32%), Positives = 189/373 (50%), Gaps = 25/373 (6%)

Query: 30  VKDVKRIIIKVGTAVVTGPNGRLAMGRLGALCEQVKQLNFEGYEVILVTSGAVGVGRQRL 89
           ++  KR+IIKVG+++VT     L    +    EQ+ QL   G EV+LV+SGAV  G QRL
Sbjct: 5   IQRAKRLIIKVGSSLVTNDGKGLDANAIARWAEQIAQLRALGKEVVLVSSGAVAEGMQRL 64

Query: 90  KYRKLVNSSFADLQNPQMDMDGKACAAVGQSVLMAIYDTLFSQLDVTSSQLLVTDRDFMD 149
            + K           P      +ACAAVGQ  L  IY+T F + D+ ++Q+L+T  D  D
Sbjct: 65  GFEK----------RPTGIHHLQACAAVGQMGLAQIYETSFRKHDLHTAQVLLTHADLAD 114

Query: 150 PSFGNQLRETVNSLLDLKVIPVFNENDAISTRRQPYEDSSGIFWDNDSLARLLAQELKAD 209
                  R T+ +LL L V+PV NEND + T           F DND+L  L+A  ++A+
Sbjct: 115 RERYLNARSTLFALLQLGVVPVINENDTVVTDEIK-------FGDNDTLGALVANLIEAE 167

Query: 210 LLIMLSDVEGLYSGPP-SDPQSKII-HTYVHEQHGKLISFGEKSRVGRGGMQAKVAAAFT 267
            LI+L+D  GL++  P  DP + +I      +   +LI+ G  + +GRGGM  K+ AA  
Sbjct: 168 ALIILTDQPGLFTADPRKDPTATLISEARAGDPSLELIAGGTGTGIGRGGMLTKILAAKR 227

Query: 268 ASSKGIPVVIASGFAIDSIIKVMRGEKIGTLFHREANQWGCSKEATAREMAVAARDC--S 325
           A++ G   VIA G     + ++  GE IGT  + E  Q    K+  A  +  A R    +
Sbjct: 228 AATSGAHTVIAWGREEQVLTRLAAGEAIGTQLNAETAQLTARKQWMADHLKTAGRVVLDA 287

Query: 326 RHLQKLSSEERKKILLDIADALE--ANEDLITSENQADLDLAQDIGYDKSLVARMTIK-- 381
             +QKLS E +  + + + +        D+IT  ++    +A+ +    S  AR  I+  
Sbjct: 288 GAVQKLSLEGKSLLPIGVVEVSGEFGRGDVITCVDENGRAIARGMSNYNSSDARRIIRHP 347

Query: 382 PGKIKSLAGSIRE 394
             +I+++ G + E
Sbjct: 348 SSEIQAILGFVEE 360


Lambda     K      H
   0.318    0.136    0.385 

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: 563
Number of extensions: 30
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: 735
Length of database: 372
Length adjustment: 35
Effective length of query: 700
Effective length of database: 337
Effective search space:   235900
Effective search space used:   235900
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: 52 (24.6 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