GapMind for catabolism of small carbon sources

 

Alignments for a candidate for put1 in Sedimenticola selenatireducens DSM 17993

Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88); Proline dehydrogenase (EC 1.5.5.2) (characterized)
to candidate WP_084610117.1 A3GO_RS0114220 bifunctional proline dehydrogenase/L-glutamate gamma-semialdehyde dehydrogenase PutA

Query= reanno::ANA3:7023590
         (1064 letters)



>NCBI__GCF_000428045.1:WP_084610117.1
          Length = 1032

 Score = 1240 bits (3208), Expect = 0.0
 Identities = 637/1031 (61%), Positives = 781/1031 (75%), Gaps = 4/1031 (0%)

Query: 33   YIVDEEQYLSELIKLVPSSDEAIERVTRRAHELVNKVRQFDKKGLMVGIDAFLQQYSLET 92
            Y VDE   L  LI L   + E +++ TR + ELV  VR  D    M  IDA L +YSL+T
Sbjct: 2    YCVDESSLLETLIPLARPTPELLKKTTRESAELVRAVRARDDAMHM--IDALLLEYSLDT 59

Query: 93   QEGIILMCLAEALLRIPDAATADALIEDKLSGAKWDEHLSKSDSVLVNASTWGLMLTGKI 152
            +EG++LMCLAE+L+RIPD+ATADALI+DKL  A W +HL +S S+LVNASTWGL+LTGK+
Sbjct: 60   REGVLLMCLAESLMRIPDSATADALIKDKLGIADWKQHLKQSKSLLVNASTWGLLLTGKV 119

Query: 153  VKLDKKIDGTPSNLLSRLVNRLGEPVIRQAMMAAMKIMGKQFVLGRTMKEALKNSEDKRK 212
            + LD  I+  P+++++RLVNRL EPV+RQAM  AMKIMG+QFVLGRT+ EAL NS  +R+
Sbjct: 120  ITLDAGIEDEPASVINRLVNRLSEPVVRQAMHQAMKIMGRQFVLGRTITEALANSRKQRE 179

Query: 213  LGYTHSYDMLGEAALTRKDAEKYFNDYANAITELGAQSYNENESPRPTISIKLSALHPRY 272
             GY++SYDMLGEAALT +DAE YF  Y+ AI  +G+ ++  + S R T+SIKLSALHPRY
Sbjct: 180  AGYSYSYDMLGEAALTDRDAEHYFEAYSGAIKAIGSDTFPSDTSFRSTVSIKLSALHPRY 239

Query: 273  EVANEDRVLTELYDTVIRLIKLARGLNIGISIDAEEVDRLELSLKLFQKLFNADATKGWG 332
            E   E RV++EL D ++ LIKLAR L++GI+IDAEE DRLELSLKLF++L+    ++GWG
Sbjct: 240  EQQQERRVISELGDRMLALIKLARELDVGITIDAEEADRLELSLKLFERLYRDQISRGWG 299

Query: 333  LLGIVVQAYSKRALPVLVWLTRLAKEQGDEIPVRLVKGAYWDSELKWAQQAGEAAYPLYT 392
             LG+VVQAY KRALPVL WL  LA +QGD IP+RL KGAYWDSE+K AQQ G  +YP++T
Sbjct: 300  NLGLVVQAYQKRALPVLFWLAALAGKQGDLIPLRLAKGAYWDSEIKHAQQLGLESYPVFT 359

Query: 393  RKAGTDVSYLACARYLLSDATRGAIYPQFASHNAQTVAAISDMAGDRNHEFQRLHGMGQE 452
            RK  TDVSYLACA +LLSD  +G IYPQFASHNA TVA++  MA    +EFQRLHGMG  
Sbjct: 360  RKEATDVSYLACASFLLSDQLKGLIYPQFASHNAHTVASVVSMATHDQYEFQRLHGMGDA 419

Query: 453  LYDTILSEAGAKAVRIYAPIGAHKDLLPYLVRRLLENGANTSFVHKLVDPKTPIESLVVH 512
            LY+ ++ E  A  VRIYAP+G+HKDLLPYLVRRLLENGAN+SFVH+L+D KTP+ESL+ H
Sbjct: 420  LYEAVI-ERYASRVRIYAPVGSHKDLLPYLVRRLLENGANSSFVHRLIDQKTPVESLIEH 478

Query: 513  PLKTLTGYKTLANNKIVLPTDIFGSDRKNSKGLNMNIISEAEPFFAALDKFKSTQWQAGP 572
            PL  L  Y +L+N +I LP DI+G  R NS G+N+N+  +  P    +  F    W A P
Sbjct: 479  PLTKLCQYSSLSNERIPLPPDIYGKGRINSCGVNINVADQWLPLQREVQAFFRQSWHAAP 538

Query: 573  LVNGQTL-TGEHKTVVSPFDTTQTVGQVAFADKAAIEQAVASADAAFATWTRTPVEVRAS 631
            L+ G+ + +GE   V +P D    VG +   D+  + QA+A A  AFA W  TPV  R+ 
Sbjct: 539  LIKGKRIESGEVVQVHAPHDRVIHVGSLIQTDEQTVGQAIAVACEAFAGWNATPVAKRSV 598

Query: 632  ALQKLADLLEENREELIALCTREAGKSIQDGIDEVREAVDFCRYYAVQAKKLMSKPELLP 691
            AL++ ADLLEE+R ELIALC  EAGK+IQD IDEVREAVDFCRYYA QA+      +LL 
Sbjct: 599  ALERAADLLEEHRAELIALCHLEAGKTIQDAIDEVREAVDFCRYYAWQARLHFDSAQLLD 658

Query: 692  GPTGELNELFLQGRGVFVCISPWNFPLAIFLGQVSAALAAGNTVVAKPAEQTSIIGYRAV 751
            GPTGE NEL+LQGRG+FVCISPWNFPLAIF GQV AALAAGN+V+AKPAEQTS+I  RAV
Sbjct: 659  GPTGEANELYLQGRGLFVCISPWNFPLAIFTGQVMAALAAGNSVIAKPAEQTSLIAARAV 718

Query: 752  QLAHQAGIPTDVLQYLPGTGATVGNALTADERIGGVCFTGSTGTAKLINRTLANREGAII 811
            +L HQAGIP  VL  LPG G+ +G  LTADERI GV FTGST TA+LINR+LA R G + 
Sbjct: 719  ELFHQAGIPDSVLHLLPGEGSRIGPLLTADERIAGVAFTGSTETARLINRSLAMRNGPVA 778

Query: 812  PLIAETGGQNAMVVDSTSQPEQVVNDVVSSSFTSAGQRCSALRVLFLQEDIADRVIDVLQ 871
             L+AETGGQNAMVVDST+ PEQV+ DV+SS+F SAGQRCSALRVLFLQ+D+A+R++ +L+
Sbjct: 779  TLVAETGGQNAMVVDSTALPEQVIKDVISSAFASAGQRCSALRVLFLQDDVAERILALLK 838

Query: 872  GAMDELVIGNPSSVKTDVGPVIDATAKANLDAHIDHIKQVGKLIKQMSLPAGTENGHFVS 931
            GAM EL +G+P  + TDVGPVID  A+  L  HI  +++   LI +  LP   E G FV+
Sbjct: 839  GAMAELKVGDPCELDTDVGPVIDEEARRTLQRHIAEMREQATLIAETPLPLNAEAGCFVA 898

Query: 932  PTAVEIDSIKVLEKEHFGPILHVIRYKASELAHVIDEINSTGFGLTLGIHSRNEGHALEV 991
            P A EI  +  L KEHFGP+LHVIR+KAS L  VI +IN++G+GLTLGIHSRNE  +  +
Sbjct: 899  PVAFEIQHMDQLSKEHFGPVLHVIRFKASRLDDVILQINNSGYGLTLGIHSRNETTSRYI 958

Query: 992  ADKVNVGNVYINRNQIGAVVGVQPFGGQGLSGTGPKAGGPHYLTRFVTEKTRTNNITAIG 1051
              +V VGNVYINRNQIGAVVGVQPFGG GLSGTGPKAGGPHYL RF TE+TRT N TAIG
Sbjct: 959  DTRVRVGNVYINRNQIGAVVGVQPFGGLGLSGTGPKAGGPHYLLRFATERTRTTNTTAIG 1018

Query: 1052 GNATLLSLGDS 1062
            GNATLLSL +S
Sbjct: 1019 GNATLLSLENS 1029


Lambda     K      H
   0.317    0.133    0.377 

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: 2422
Number of extensions: 91
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: 1064
Length of database: 1032
Length adjustment: 45
Effective length of query: 1019
Effective length of database: 987
Effective search space:  1005753
Effective search space used:  1005753
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: 58 (26.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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