GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serB in Ammonifex degensii KC4

Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate WP_012818167.1 ADEG_RS00050 phosphoglycerate dehydrogenase

Query= reanno::Cola:Echvi_2777
         (630 letters)



>NCBI__GCF_000024605.1:WP_012818167.1
          Length = 527

 Score =  200 bits (508), Expect = 1e-55
 Identities = 128/359 (35%), Positives = 198/359 (55%), Gaps = 18/359 (5%)

Query: 235 VLLLENVHPIGVEIMKQEGYNVEV-VSSAMSEEELCEKIKNVSIIGIRSKTQITKKVLEN 293
           VL+ + V P G++ +  E  +VEV     ++EEEL E I     + +RS T++T  VLE 
Sbjct: 4   VLVTDGVSPEGLKALT-EAPDVEVDFRPTLNEEELKEIIGEYDALIVRSATKVTAAVLEK 62

Query: 294 ANRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRNLHDKTL 353
           A RL  +G   +G + ID++    KGI V NAP  NT +  E  I  ++ L RN+ +   
Sbjct: 63  ARRLKIIGRAGVGVDNIDVKAATAKGIIVANAPGGNTVAAAEHTIGLMLSLARNIPEACA 122

Query: 354 KMHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYD--IVERLALGN 411
           +   G+W++ +    E+RGK LGIIG G IG++++  A+ M M +  YD  I E  A   
Sbjct: 123 RTKSGVWDRKSFMGVELRGKVLGIIGLGRIGSEVAKRAQAMEMKIIAYDPYIPEERARDL 182

Query: 412 ATKIDSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHVVDVPALR 471
             K+  LD LL+  D I++H+    E  +++++E   KMK G  L+N +RG +VD  AL 
Sbjct: 183 RVKLVPLDTLLQEADFITIHIPLSKETYHLIDREAFVKMKPGVRLINCARGGIVDEEALY 242

Query: 472 DALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIGGSTLEAQENIAQFVPG 531
           +AL+ G +AGAA+DVF  EP  +       L   PN ++TPH+G ST+EAQ  +A+ +  
Sbjct: 243 EALKEGKVAGAALDVFEKEPVTS-----HPLFSLPNVVVTPHLGASTVEAQLAVAEVIAQ 297

Query: 532 KIIEYINSGNTFNSVNFPNIQL-------PFLKDAHRLIHIHQNAPGVLAKINQVLASY 583
           +++  +  G   ++VN P ++        PFL  A +L      A  V  +INQV  +Y
Sbjct: 298 EVLTALRGGFVRHAVNLPYLRPEVLPVVGPFLPLAEKLGLF--AAQLVSGRINQVEVNY 354


Lambda     K      H
   0.317    0.136    0.377 

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: 654
Number of extensions: 26
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: 630
Length of database: 527
Length adjustment: 36
Effective length of query: 594
Effective length of database: 491
Effective search space:   291654
Effective search space used:   291654
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: 53 (25.0 bits)

This GapMind analysis is from Apr 10 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