GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Rhizobium johnstonii 3841

Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate WP_011650233.1 RL_RS02310 alpha-hydroxy acid oxidase

Query= reanno::WCS417:GFF3737
         (376 letters)



>NCBI__GCF_000009265.1:WP_011650233.1
          Length = 382

 Score =  243 bits (621), Expect = 5e-69
 Identities = 153/372 (41%), Positives = 200/372 (53%), Gaps = 8/372 (2%)

Query: 8   DYRAAAKRKLPRFLFDYIDGGAYAEHTLRANSSDLAEISLRQRILRNVDNLSLKTTLFGQ 67
           D+R  AKR+LP  +FDYIDGGA  E T R N++      L   +LR V ++ +  T+ GQ
Sbjct: 11  DFRRMAKRRLPGPIFDYIDGGADDEVTYRRNTAAFEACDLVPDVLRGVADVDMSVTVMGQ 70

Query: 68  ELDMPVILSPVGLTGMYARRGEVQAAKAAANKGIPFCLSTVSVCPIEEVASQSAQAIWFQ 127
           +L MPV  SP  L  ++  +GE   A AAA  G  F +S++    +EE    S     +Q
Sbjct: 71  KLAMPVYCSPTALQRLFHHQGERAVAAAAAKHGTMFGVSSLGTISLEEARQISNGPQVYQ 130

Query: 128 LYVLKDRGFMRNALERAQAAGVTTLVFTVDMPTPGARYRDAHSGMSGPFAAQRR-MLQAV 186
            Y  KDRG  R  + RA+ AGV  ++ TVD  T G R RD  +G + PF      M Q  
Sbjct: 131 FYFHKDRGLNREMMARAKNAGVQAMMLTVDSITGGNRERDKRTGFAIPFKLNLAGMTQFA 190

Query: 187 TKPQWAFD--VGLMGRPHDLGNISKYLGKPTHLEDYIGWLANNFDASISWKDL-EWIREF 243
            KP WA D       R   L N  K  G    +  Y        D S+SW D+ E +RE 
Sbjct: 191 VKPSWAIDWLTHERFRLPQLENHVKMDGGALSISRYF---TEMLDPSMSWDDVAEMVRE- 246

Query: 244 WKGPMIIKGILDPQDAKDAVSFGADGIVVSNHGGRQLDGVLSTAKALPPIADAVGDDLTV 303
           W GP  +KGI+  +DAK A   G  GIV+SNHGGRQLDG  S    L  I DAVGD + V
Sbjct: 247 WGGPFCLKGIMSVEDAKRAAEIGCSGIVLSNHGGRQLDGSRSAFDQLAEIVDAVGDRIDV 306

Query: 304 LVDSGIRSGLDVVRMLALGAKACLLGRATAYALAADGQHGVENLLDIFAKEMRVAMTLTG 363
           ++D G++ G  V++ L+LGAKA  LGR   + LAA GQ GVE  L+    E+   M L G
Sbjct: 307 MMDGGVQRGTHVLKALSLGAKAVGLGRYYLFPLAAAGQPGVERALETMRTEIERGMKLMG 366

Query: 364 VTSIAQIDRSTL 375
            TS++Q+ R  L
Sbjct: 367 CTSVSQLTRRNL 378


Lambda     K      H
   0.321    0.136    0.401 

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: 355
Number of extensions: 9
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: 376
Length of database: 382
Length adjustment: 30
Effective length of query: 346
Effective length of database: 352
Effective search space:   121792
Effective search space used:   121792
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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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