GapMind for Amino acid biosynthesis

 

Alignments for a candidate for mesB in Desulfatiglans anilini DSM 4660

Align [corrinoid iron-sulfur protein]-dependent methionine synthase (characterized)
to candidate WP_028321197.1 H567_RS0109315 hypothetical protein

Query= metacyc::MONOMER-21502
         (342 letters)



>NCBI__GCF_000422285.1:WP_028321197.1
          Length = 350

 Score =  235 bits (600), Expect = 1e-66
 Identities = 129/339 (38%), Positives = 191/339 (56%), Gaps = 12/339 (3%)

Query: 5   DFHFLPTMIGSMPHTDPKAAVDIITHYLQDIPVWPQLPRRSCLEGMSAQFSQGLP--GVK 62
           DFHF+ T IGS+P TD  +  + I      +P WPQ PRRS +E MS QFS+G+P     
Sbjct: 7   DFHFIATGIGSVPFTDIASTCNGILREAPRMPFWPQFPRRSPVEDMSIQFSEGMPLLSAD 66

Query: 63  INQDKVWIEPNPSFESELESLYQAYLDNDFNKFPIGAEYAAGLY----ELASRNLSPL-L 117
           +    + I+ +      L + Y  ++ +D   F +  EYA GLY     LA R       
Sbjct: 67  LENRSLAIDSDTPQADALVAFYDRFMSHDVEAFALSREYAPGLYWMADSLADRPADEGGF 126

Query: 118 VKGHITGPLTYCMSIKDPSGKDILYDEVLSDAATKLLKLKATWQEHFLRNICRNTIIFVD 177
            KG   GP+T+   I+D +G  +L++  L +A T  L +KA WQ   L +  R  +IF+D
Sbjct: 127 FKGQTVGPVTFAAGIRDTNGTSVLHNPELLEALTHALAIKARWQVGALASSGRQPVIFLD 186

Query: 178 EPAMSAYGSAYLPLSREQVTGMF----DEVFSGISGLKGVHCCGNTDWSILMDTRVDIIN 233
           EP +S +GSA+ P+ RE V  +     D + +    L G+HCCGNTDWS++++   DI+N
Sbjct: 187 EPYLSGFGSAFSPIQRETVIELLRIVIDYLRTHTDTLIGIHCCGNTDWSMILEAEPDIVN 246

Query: 234 FDTYAYANSLSIYTDEVKAFIKRGGAVAWGIVPTDEKALKEETAASLKDRLEAAMSHFDS 293
           FD + + +   +Y D ++ F+  GGAVAWGIVPT   A+ E T  SL  RL   +++ + 
Sbjct: 247 FDAFEHLDYFLLYPDHIRKFLLAGGAVAWGIVPT-SPAVMEATFDSLASRLRKGLAYLEE 305

Query: 294 HGLPFAELARHSLITPACGLGLKSPEAAERAPQLLAELS 332
            G+  + LA+ SL+TPACG+G  +   A +A +LL  LS
Sbjct: 306 KGIDRSLLAQRSLLTPACGMGSMTEREARKALELLGMLS 344


Lambda     K      H
   0.319    0.135    0.409 

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: 312
Number of extensions: 15
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: 342
Length of database: 350
Length adjustment: 29
Effective length of query: 313
Effective length of database: 321
Effective search space:   100473
Effective search space used:   100473
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 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