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_027490423.1 LRK54_RS10365 homoserine dehydrogenase

Query= SwissProt::Q5B998
         (368 letters)



>NCBI__GCF_021560695.1:WP_027490423.1
          Length = 381

 Score =  214 bits (545), Expect = 3e-60
 Identities = 148/365 (40%), Positives = 204/365 (55%), Gaps = 20/365 (5%)

Query: 7   LGVIGVGGVGTAFLNQLARLPNAPKLILLARSSQTLLSPTPSYSPTIPA--AEWKTAVET 64
           +GVIG G VG+A L QL      P+L+  +     L     S    +    AE  +    
Sbjct: 30  VGVIGPGRVGSALLEQLRAAQ--PRLLRDSALELKLCGVVASKRMWLDCDDAELNSRHGG 87

Query: 65  PSLTKSGALTPDEIATYLASAPGR-SILVDNTSDPALASNYPVFLRKGISVVTPNKKGFS 123
             + +   L  D  A ++  + GR ++L+D +++  +A+ YP +L  G+ VVTPNK   S
Sbjct: 88  AQIWRPNDL--DTFAGHVRGSDGRHALLIDCSANDEVAARYPRWLAAGLHVVTPNKLAGS 145

Query: 124 SDLSLWKEIFAAAAEGKALVYHESTVGAGLPVISTLKDLVNTGDEVTRIEGVFSGTLSFL 183
             LS W+ I  A A G    Y E+TV AGLPV+ TL+DL++TGD++  ++G+FSGTL++L
Sbjct: 146 GPLSRWQAIRTACAGGARFRY-EATVCAGLPVVQTLRDLLDTGDDLLAVDGMFSGTLAWL 204

Query: 184 FNTFAPASGSSSAKWSEVVSQAKELGYTEPDPRDDLNGMDVARKLTILARIAGLDVQSPD 243
            N            +S +V +A  LGYTEPDPRDDL+G+DVARKL ILAR AG    S +
Sbjct: 205 CNRH-----DGRQPFSALVREAHALGYTEPDPRDDLSGLDVARKLVILAREAG-QALSLE 258

Query: 244 SFPIESLIPAELTSLPSSADGIAQFMARLPEFDSQMAAIKEGAEKAGKVVRYVGSVDVAK 303
              ++SL+P  L +LP     +   M RL E D+ MAA    A   G V+R+V  +D   
Sbjct: 259 DVDLQSLVPPALAALP-----LDDCMRRLDELDAPMAAKLAEARAEGGVLRHVAQLD-RH 312

Query: 304 KEVRVGLQQFDKDSAIAGLKGSDNIISFYTRRYGSNPLIVQGAGAGGDVTAMGVTADLLK 363
               V L       A A  + +DNI+ F TRRY  NPLIVQG GAG +VTA GV  DLL+
Sbjct: 313 GRASVRLLVLPASHAFAHTRLTDNIVQFSTRRYCDNPLIVQGPGAGPEVTAAGVFTDLLR 372

Query: 364 VIERL 368
           + E L
Sbjct: 373 IAESL 377


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: 305
Number of extensions: 16
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: 368
Length of database: 381
Length adjustment: 30
Effective length of query: 338
Effective length of database: 351
Effective search space:   118638
Effective search space used:   118638
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: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

Links

Downloads

Related tools

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