GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Ss in Halomonas desiderata SP1

Align MalK, component of Maltose and maltooligosaccharide porter (characterized)
to candidate WP_086508118.1 BZY95_RS00870 ABC transporter ATP-binding protein

Query= TCDB::Q97UG5
         (617 letters)



>NCBI__GCF_002151265.1:WP_086508118.1
          Length = 766

 Score =  451 bits (1160), Expect = e-131
 Identities = 246/623 (39%), Positives = 378/623 (60%), Gaps = 19/623 (3%)

Query: 8   LLKVNELTAGYFNQDGFVIGVTNVNFEVYPNEIFAIAGESGCGKSTLAMAIYGLLKYPGV 67
           LLKV +L   Y    G V  V  ++F++ P E   + GESGCGK+T A A+  LL   G 
Sbjct: 6   LLKVEDLAIHYRTGAGPVQAVDGIHFDLRPGEALGLVGESGCGKTTAAKAMLRLLPPNGE 65

Query: 68  VLRGHVYLKDKDILSITQEELRKLRMKEFVYVPQFAMDALDPVAKIGDQMMRAAVSH-GV 126
           V RG +    +D++++ +E +RK+R KE  ++ Q AM+ALDPV  +GDQ++ A  +H  +
Sbjct: 66  VPRGRIDFDGRDLVALDEESMRKVRWKEIAWISQAAMNALDPVYTVGDQILEAMNAHIKI 125

Query: 127 NVEEARKLIKEKLELVDLPYNVVNMYPHELSGGMRQRVVIATSILLNPSLIILDEPTTGL 186
           + + A    +E    V +    ++ YPHE+SGGM+QR VIA ++ L+P LII DEPTT L
Sbjct: 126 DRKTAWAHAEELFRAVGIDPGRLSAYPHEMSGGMKQRAVIAMALALDPKLIIADEPTTAL 185

Query: 187 DVIVQYEILKDLKRIQRQLGVSLVIISHDISMLLMISDRVGIMYAGEIVEIGSKEEIIKR 246
           DV+ Q +IL  L +++R+ G+ L+ I+HDIS+++   DRV +MY G I+E G   E+   
Sbjct: 186 DVVTQAQILARLSKLRRERGMGLLFITHDISVVVQTCDRVAVMYGGHIMETGPVREVFGT 245

Query: 247 PSHPYTYLLISSLPSLVKRREKLLSIPGNPPLMLSKVPNSCRFYDRCPFKMEKCSTLNPA 306
           P HPYT  L ++ P+L   + +L+SIPG+PP +L+  P+ CRF +RCPF  E+C    P 
Sbjct: 246 PFHPYTMGLTNAFPTLEGAQRELISIPGSPPDLLNP-PSGCRFAERCPFATERCVRETPP 304

Query: 307 LGDIMDGHKARCFL--QKGGYVDLSTLPIPLEYYAEEKAE-TDLSESNQH-----EVVMK 358
           L  + +  +A C    Q   +   + L        E   E    + S +H      ++++
Sbjct: 305 LHPVGEERQAACHYPDQAEAFRVKAALNETWAVVGERLNEPVQGAGSIEHLETEAPLLLE 364

Query: 359 ILNLSKIYYIRKNLI-------LSEPINAVNDVSFELKKGTITALVGGSGHGKSTIAKIL 411
           +  L K + + +  +           ++AV+ +SF+L++G I  L G SG GK+T  ++L
Sbjct: 365 VEELKKHFPVEQGFLDGLRGRNKDRKVHAVDGISFDLREGEILGLAGESGSGKTTTGEML 424

Query: 412 AGMIQQTSGKIILLGKDVSEYGVRNSMWYKENVQMIFQDPYSSLDPRHTVRWHVERPLLI 471
             ++  T G+I   G D+++   R    ++   QMIFQDPY +L+PR T+   V  PL+I
Sbjct: 425 VRLLDVTEGEIRFEGADIAQLTGRELKTFRRRAQMIFQDPYQTLNPRFTIFDIVAEPLII 484

Query: 472 HKKVSNKDQLLPKIIEVLKNVGLKPPEKYLYKYPHELSGGERQRVAIARATAVEPKVLVA 531
           H +++  + L  K++  L+  GLKP E Y  ++PHELSGG+RQRVAIARA  +EP+ +VA
Sbjct: 485 H-RLAEGEALRQKVVVALERAGLKPAEVYAERFPHELSGGQRQRVAIARAIVLEPRFIVA 543

Query: 532 DEPVSMLDASLRAGILNLIKKFKKN-GISILYITHDIATVNYIADEIMVIYKGRIVEKGN 590
           DEPVSMLD S+RAG+LNL+ +F+   GIS +Y++HD+ T+ Y+AD   ++Y G IVE G 
Sbjct: 544 DEPVSMLDVSIRAGVLNLMHRFRNELGISFVYVSHDLPTIRYVADRTAIMYLGEIVEVGP 603

Query: 591 TYEVISNPSHEYTKRLIEAVPDP 613
           T +V+    H YT+ L+EA P+P
Sbjct: 604 TEQVVRERKHPYTQLLLEASPEP 626



 Score =  160 bits (406), Expect = 1e-43
 Identities = 104/288 (36%), Positives = 154/288 (53%), Gaps = 16/288 (5%)

Query: 20  NQDGFVIGVTNVNFEVYPNEIFAIAGESGCGKSTLAMAIYGLLKYPGVVLRGHVYLKDKD 79
           N+D  V  V  ++F++   EI  +AGESG GK+T    +  LL     V  G +  +  D
Sbjct: 386 NKDRKVHAVDGISFDLREGEILGLAGESGSGKTTTGEMLVRLLD----VTEGEIRFEGAD 441

Query: 80  ILSITQEELRKLRMKEFVYVPQFAMDALDPVAKIGDQMMRAAVSHGVNVEEA-RKLIKEK 138
           I  +T  EL+  R +  + + Q     L+P   I D +    + H +   EA R+ +   
Sbjct: 442 IAQLTGRELKTFRRRAQM-IFQDPYQTLNPRFTIFDIVAEPLIIHRLAEGEALRQKVVVA 500

Query: 139 LELVDL-PYNV-VNMYPHELSGGMRQRVVIATSILLNPSLIILDEPTTGLDVIVQYEILK 196
           LE   L P  V    +PHELSGG RQRV IA +I+L P  I+ DEP + LDV ++  +L 
Sbjct: 501 LERAGLKPAEVYAERFPHELSGGQRQRVAIARAIVLEPRFIVADEPVSMLDVSIRAGVLN 560

Query: 197 DLKRIQRQLGVSLVIISHDISMLLMISDRVGIMYAGEIVEIGSKEEIIKRPSHPYTYLLI 256
            + R + +LG+S V +SHD+  +  ++DR  IMY GEIVE+G  E++++   HPYT LL+
Sbjct: 561 LMHRFRNELGISFVYVSHDLPTIRYVADRTAIMYLGEIVEVGPTEQVVRERKHPYTQLLL 620

Query: 257 SSL----PSLVKRREKLLSIPGNPPLMLSKVPNSCRFYDRCPFKMEKC 300
            +     P++VK     L   G  P  + + PN C F+ RCP  M  C
Sbjct: 621 EASPEPDPAVVK---PPLESAGEIPSAV-EPPNGCHFHTRCPRAMAHC 664


Lambda     K      H
   0.319    0.138    0.391 

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: 1092
Number of extensions: 48
Number of successful extensions: 13
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 4
Number of HSP's successfully gapped: 4
Length of query: 617
Length of database: 766
Length adjustment: 39
Effective length of query: 578
Effective length of database: 727
Effective search space:   420206
Effective search space used:   420206
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 (21.7 bits)
S2: 54 (25.4 bits)

This GapMind analysis is from Sep 24 2021. 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