GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hom in Rhodanobacter denitrificans FW104-10B01

Align Homoserine dehydrogenase; HDH; EC 1.1.1.3 (characterized)
to candidate WP_027490863.1 LRK54_RS05300 homoserine dehydrogenase

Query= SwissProt::Q5B998
         (368 letters)



>NCBI__GCF_021560695.1:WP_027490863.1
          Length = 360

 Score =  190 bits (483), Expect = 5e-53
 Identities = 135/367 (36%), Positives = 198/367 (53%), Gaps = 32/367 (8%)

Query: 2   SAPIYLGVIGVGGVGTAFLNQL-ARLPNAPKLILLARSSQTLLSPTPSYSPTIPAAEWKT 60
           S+ I + ++G G VG A L  L      + +L+  A S +    P       +       
Sbjct: 17  SSAIAIVLLGTGVVGGALLKLLNTSAAGSLRLVGAANSRRQQTDPLSLAQRNL------- 69

Query: 61  AVETPSLTKSGALTPDEIATYLASAPGRS----ILVDNTSDPALASNYPVFLRKGISVVT 116
                 L + GA  P + A+ LA+  G +    ++VD T+   LA+ +  +L +G  VVT
Sbjct: 70  ---REQLNQHGA--PRDNASLLAALDGSAAAVKVIVDATASTVLAARHAEWLARGYHVVT 124

Query: 117 PNKKGFSSDLSLWKEIFAAAAEGKALVYHES-TVGAGLPVISTLKDLVNTGDEVTRIEGV 175
            NK     +LS W+ + AA A G    Y +S TVGAGLPV+STL+ L   GD +  +EGV
Sbjct: 125 ANKALAGGELSGWRALQAALANGGR--YGDSATVGAGLPVLSTLRRLRRCGDGLLTLEGV 182

Query: 176 FSGTLSFLFNTFAPASGSSSAKWSEVVSQAKELGYTEPDPRDDLNGMDVARKLTILARIA 235
           FSG+LS+LFN +       S  +SE++ +A++LGYTEPDPR DL+G DVARKL I+AR A
Sbjct: 183 FSGSLSWLFNQY-----DGSRPFSELLREARQLGYTEPDPRSDLSGEDVARKLLIIARNA 237

Query: 236 GLDVQSPDSFPIESLIPAELTSLPSSADGIAQFMARLPEFDSQMAAIKEGAEKAGKVVRY 295
           G  +   D   ++ L+P  L  L + A     F+ RL E D+ +AA    A   G V+R+
Sbjct: 238 GFAL-GTDEVQVDGLVPEALRGLSTEA-----FLTRLEELDAPLAARHAAASSRGCVLRF 291

Query: 296 VGSVDVAKKEVRVGLQQFDKDSAIAGLKGSDNIISFYTRRYGSNPLIVQGAGAGGDVTAM 355
           +  ++  +   RVGL +       A L G+DN  +  T RY + PL++QG GAG +VTA 
Sbjct: 292 LARLN-QRGHARVGLAEVPLTHPAARLYGTDNQFALTTTRYHAQPLVIQGPGAGPEVTAQ 350

Query: 356 GVTADLL 362
            +  D+L
Sbjct: 351 ALLGDVL 357


Lambda     K      H
   0.314    0.132    0.368 

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: 279
Number of extensions: 11
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: 368
Length of database: 360
Length adjustment: 29
Effective length of query: 339
Effective length of database: 331
Effective search space:   112209
Effective search space used:   112209
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 49 (23.5 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