Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H555
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009249 | protein lipoylation | 5 | 8 |
GO:0018193 | peptidyl-amino acid modification | 5 | 8 |
GO:0018205 | peptidyl-lysine modification | 6 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0036211 | protein modification process | 4 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0051604 | protein maturation | 4 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016874 | ligase activity | 2 | 8 |
GO:0016746 | acyltransferase activity | 3 | 1 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 1 |
GO:0017118 | lipoyltransferase activity | 5 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 1 |
GO:0016979 | lipoate-protein ligase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.343 |
DEG_APCC_DBOX_1 | 261 | 269 | PF00400 | 0.345 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.491 |
DEG_SCF_FBW7_1 | 383 | 390 | PF00400 | 0.497 |
DEG_SPOP_SBC_1 | 529 | 533 | PF00917 | 0.288 |
DOC_ANK_TNKS_1 | 288 | 295 | PF00023 | 0.495 |
DOC_CKS1_1 | 384 | 389 | PF01111 | 0.538 |
DOC_CYCLIN_RxL_1 | 133 | 142 | PF00134 | 0.439 |
DOC_CYCLIN_RxL_1 | 250 | 260 | PF00134 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 134 | 140 | PF00134 | 0.439 |
DOC_MAPK_FxFP_2 | 163 | 166 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 353 | 359 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 543 | 550 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 329 | 338 | PF00069 | 0.470 |
DOC_MIT_MIM_1 | 540 | 548 | PF04212 | 0.412 |
DOC_PP1_RVXF_1 | 11 | 17 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 260 | 267 | PF00149 | 0.355 |
DOC_PP1_RVXF_1 | 46 | 52 | PF00149 | 0.460 |
DOC_PP4_FxxP_1 | 163 | 166 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.296 |
DOC_USP7_UBL2_3 | 517 | 521 | PF12436 | 0.430 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.363 |
LIG_14-3-3_CanoR_1 | 122 | 127 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 227 | 232 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 253 | 258 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 348 | 357 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 413 | 423 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 465 | 469 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 556 | 561 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 600 | 606 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 633 | 640 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 95 | 102 | PF00244 | 0.507 |
LIG_APCC_ABBAyCdc20_2 | 354 | 360 | PF00400 | 0.446 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 46 | 50 | PF00533 | 0.440 |
LIG_Clathr_ClatBox_1 | 480 | 484 | PF01394 | 0.397 |
LIG_deltaCOP1_diTrp_1 | 522 | 530 | PF00928 | 0.439 |
LIG_DLG_GKlike_1 | 122 | 129 | PF00625 | 0.463 |
LIG_eIF4E_1 | 377 | 383 | PF01652 | 0.513 |
LIG_eIF4E_1 | 634 | 640 | PF01652 | 0.323 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.473 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.437 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.519 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.297 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.372 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.469 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.446 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.384 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.334 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.491 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.492 |
LIG_FHA_1 | 666 | 672 | PF00498 | 0.379 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.491 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.507 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.283 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.329 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.390 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.483 |
LIG_GBD_Chelix_1 | 150 | 158 | PF00786 | 0.443 |
LIG_LIR_Apic_2 | 161 | 166 | PF02991 | 0.456 |
LIG_LIR_Apic_2 | 522 | 528 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 398 | 409 | PF02991 | 0.467 |
LIG_LIR_LC3C_4 | 229 | 233 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 549 | 554 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.463 |
LIG_NRBOX | 634 | 640 | PF00104 | 0.438 |
LIG_Pex14_1 | 630 | 634 | PF04695 | 0.381 |
LIG_REV1ctd_RIR_1 | 48 | 54 | PF16727 | 0.474 |
LIG_SH2_CRK | 525 | 529 | PF00017 | 0.426 |
LIG_SH2_GRB2like | 267 | 270 | PF00017 | 0.316 |
LIG_SH2_NCK_1 | 525 | 529 | PF00017 | 0.438 |
LIG_SH2_SRC | 394 | 397 | PF00017 | 0.281 |
LIG_SH2_STAT3 | 200 | 203 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.406 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.341 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.488 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.384 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.424 |
LIG_SUMO_SIM_anti_2 | 482 | 487 | PF11976 | 0.241 |
LIG_SUMO_SIM_par_1 | 380 | 386 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 531 | 538 | PF11976 | 0.333 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.500 |
LIG_TRFH_1 | 200 | 204 | PF08558 | 0.497 |
LIG_WRC_WIRS_1 | 165 | 170 | PF05994 | 0.470 |
MOD_CDK_SPxxK_3 | 17 | 24 | PF00069 | 0.492 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.488 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.437 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.617 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.511 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.403 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.407 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.452 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.456 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.377 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.381 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.429 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.447 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.481 |
MOD_Cter_Amidation | 360 | 363 | PF01082 | 0.363 |
MOD_Cter_Amidation | 499 | 502 | PF01082 | 0.423 |
MOD_DYRK1A_RPxSP_1 | 114 | 118 | PF00069 | 0.499 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.489 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.304 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.282 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.490 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.541 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.340 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.534 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.307 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.441 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.544 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.362 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.260 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.465 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.436 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.399 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.393 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.408 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.386 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.623 |
MOD_LATS_1 | 120 | 126 | PF00433 | 0.468 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.363 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.368 |
MOD_N-GLC_2 | 313 | 315 | PF02516 | 0.316 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.603 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.506 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.537 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.263 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.256 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.440 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.391 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.450 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.439 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.391 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.508 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.339 |
MOD_NEK2_2 | 431 | 436 | PF00069 | 0.264 |
MOD_OFUCOSY | 144 | 149 | PF10250 | 0.442 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.483 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.256 |
MOD_PK_1 | 405 | 411 | PF00069 | 0.357 |
MOD_PKA_1 | 299 | 305 | PF00069 | 0.298 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.305 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.420 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.295 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.282 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.407 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.394 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.515 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.378 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.354 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.342 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.350 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.276 |
MOD_Plk_1 | 655 | 661 | PF00069 | 0.533 |
MOD_Plk_2-3 | 507 | 513 | PF00069 | 0.474 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.463 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.448 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.499 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.282 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.437 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.408 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.391 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.285 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.488 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.474 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.490 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.388 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.468 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.404 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.368 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.352 |
MOD_SUMO_rev_2 | 356 | 364 | PF00179 | 0.206 |
TRG_DiLeu_BaLyEn_6 | 259 | 264 | PF01217 | 0.377 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.366 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 543 | 545 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 607 | 609 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.521 |
TRG_NES_CRM1_1 | 540 | 553 | PF08389 | 0.460 |
TRG_NLS_MonoExtN_4 | 55 | 62 | PF00514 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 253 | 258 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 393 | 398 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 462 | 466 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I310 | Leptomonas seymouri | 59% | 100% |
A0A0S4IZJ4 | Bodo saltans | 33% | 100% |
A0A3R7MGW3 | Trypanosoma rangeli | 39% | 100% |
A0A3S5H615 | Leishmania donovani | 78% | 100% |
E9ALC5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QII0 | Leishmania major | 79% | 100% |