GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Desulfovibrio vulgaris Miyazaki F

Align isocitrate-homoisocitrate dehydrogenase (EC 1.1.1.286) (characterized)
to candidate 8501002 DvMF_1739 isocitrate/isopropylmalate dehydrogenase (RefSeq)

Query= BRENDA::Q4J6C9
         (411 letters)



>FitnessBrowser__Miya:8501002
          Length = 382

 Score =  353 bits (905), Expect = e-102
 Identities = 170/370 (45%), Positives = 251/370 (67%), Gaps = 4/370 (1%)

Query: 29  ILYIEGDGIGPEITNSAIRVVNKAVEKAYKSSREIKWLEVYAGEKANKITGDRFPKETQD 88
           + +IEGDGIGP++  +A  V++ AV K Y  +R I+W E+ AGEKA   TG+  P+ T  
Sbjct: 5   VYWIEGDGIGPDVWKAARPVIDAAVAKTYGDARSIEWKELLAGEKAYAATGEYLPEATMQ 64

Query: 89  MLLKYRVVLKGPLETPIGKGWKSINVAIRLMLDLYANIRPVKYIEGLESPLKHPEKVDMI 148
            L    + +KGPL TP+GKG++S+NV +R  LDLYA IRP++Y EG+ SP+K P+ VDM+
Sbjct: 65  ALRGAELAIKGPLGTPVGKGFRSLNVTLRQTLDLYACIRPIRYFEGIMSPVKRPDLVDMV 124

Query: 149 IFRENTDDLYRGIEFPYDSEEAKKIRKFLREELKVDIEDDTGIGLKVMSKFKTQRITRLA 208
           +FRENT+D+Y GIE+   + EAK++  FLR EL  +++ ++ +G+K M+   ++R+ R A
Sbjct: 125 VFRENTEDVYAGIEYKAGTPEAKRLIDFLRNELGANVDPESAVGIKPMTARGSKRLVRRA 184

Query: 209 LNYALQNSRKKVTVMHKGNVMKYTEGSFREWAYEVALNEYRDKIVTEEEINRGVNSEGKV 268
           +++A+   R  +T++HKGN+MK+TEG FREW YEV  +E+ D  V E +      + GKV
Sbjct: 185 MDFAVAQKRSSLTLVHKGNIMKFTEGGFREWGYEVVRDEFADAAVLEADAG---GAAGKV 241

Query: 269 ILNDRIADNMLQQIIIRPDEYDIILAPNVNGDYISDAAGALIGNIGMLGGANIGDTGGMF 328
           ++ DRIAD M Q+++IRPD+Y +I   N+NGDY+SDA  A +G +G+  G N+ D+   F
Sbjct: 242 VVKDRIADAMFQEVLIRPDQYSVIATSNLNGDYLSDALAAQVGGLGLAPGVNMSDSLAFF 301

Query: 329 EAIHGTAPKYAGKNVANPTGIIKSCELMLYFMGWSEAARLIEKAINESIKQKKVTQDIAR 388
           EA HGTAP  AG++ ANP  +I    LML  MGW++AA  I  AIN +I ++ VT D+A 
Sbjct: 302 EATHGTAPTIAGQDKANPGSLILCGALMLEHMGWNDAATRIYNAINTTIGKRTVTVDLAS 361

Query: 389 YL-GITPLGT 397
            +   T +GT
Sbjct: 362 QMASATTVGT 371


Lambda     K      H
   0.317    0.137    0.394 

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: 381
Number of extensions: 11
Number of successful extensions: 2
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: 411
Length of database: 382
Length adjustment: 31
Effective length of query: 380
Effective length of database: 351
Effective search space:   133380
Effective search space used:   133380
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: 50 (23.9 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