Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016874 | ligase activity | 2 | 6 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 6 |
GO:0016880 | acid-ammonia (or amide) ligase activity | 4 | 6 |
GO:0047479 | trypanothione synthase activity | 5 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.260 |
CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.513 |
CLV_C14_Caspase3-7 | 561 | 565 | PF00656 | 0.443 |
CLV_C14_Caspase3-7 | 89 | 93 | PF00656 | 0.371 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.541 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 577 | 579 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.581 |
DEG_APCC_DBOX_1 | 254 | 262 | PF00400 | 0.456 |
DEG_MDM2_SWIB_1 | 62 | 69 | PF02201 | 0.344 |
DOC_CYCLIN_yCln2_LP_2 | 636 | 642 | PF00134 | 0.594 |
DOC_MAPK_gen_1 | 485 | 493 | PF00069 | 0.443 |
DOC_MAPK_JIP1_4 | 231 | 237 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 197 | 206 | PF00069 | 0.569 |
DOC_PP1_RVXF_1 | 395 | 401 | PF00149 | 0.443 |
DOC_PP2B_LxvP_1 | 636 | 639 | PF13499 | 0.430 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.381 |
DOC_PP4_FxxP_1 | 212 | 215 | PF00568 | 0.538 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.443 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.275 |
DOC_USP7_UBL2_3 | 163 | 167 | PF12436 | 0.337 |
DOC_USP7_UBL2_3 | 479 | 483 | PF12436 | 0.443 |
DOC_USP7_UBL2_3 | 643 | 647 | PF12436 | 0.524 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 222 | 226 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 313 | 319 | PF00244 | 0.538 |
LIG_BIR_III_2 | 124 | 128 | PF00653 | 0.307 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.539 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.443 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.275 |
LIG_deltaCOP1_diTrp_1 | 308 | 318 | PF00928 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 495 | 502 | PF00928 | 0.443 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.371 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.443 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.443 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.443 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.485 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.495 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.462 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.275 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.454 |
LIG_LIR_Apic_2 | 209 | 215 | PF02991 | 0.536 |
LIG_LIR_Apic_2 | 498 | 504 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 10 | 19 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 139 | 149 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 168 | 179 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 407 | 418 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 495 | 505 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 592 | 603 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 623 | 633 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 97 | 104 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 10 | 14 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 495 | 500 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 503 | 509 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 592 | 598 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 623 | 629 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.378 |
LIG_MLH1_MIPbox_1 | 208 | 212 | PF16413 | 0.370 |
LIG_MYND_3 | 1 | 5 | PF01753 | 0.501 |
LIG_NRBOX | 487 | 493 | PF00104 | 0.443 |
LIG_Pex14_1 | 154 | 158 | PF04695 | 0.468 |
LIG_Pex14_1 | 497 | 501 | PF04695 | 0.443 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.526 |
LIG_Pex14_2 | 329 | 333 | PF04695 | 0.443 |
LIG_Pex14_2 | 502 | 506 | PF04695 | 0.443 |
LIG_Pex14_2 | 51 | 55 | PF04695 | 0.351 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.360 |
LIG_Rb_LxCxE_1 | 336 | 355 | PF01857 | 0.275 |
LIG_Rb_pABgroove_1 | 426 | 434 | PF01858 | 0.443 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.443 |
LIG_SH2_CRK | 582 | 586 | PF00017 | 0.443 |
LIG_SH2_CRK | 595 | 599 | PF00017 | 0.300 |
LIG_SH2_GRB2like | 33 | 36 | PF00017 | 0.494 |
LIG_SH2_GRB2like | 520 | 523 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 595 | 599 | PF00017 | 0.443 |
LIG_SH2_PTP2 | 141 | 144 | PF00017 | 0.381 |
LIG_SH2_SRC | 25 | 28 | PF00017 | 0.510 |
LIG_SH2_SRC | 595 | 598 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 410 | 414 | PF00017 | 0.443 |
LIG_SH2_STAT3 | 279 | 282 | PF00017 | 0.443 |
LIG_SH2_STAT3 | 414 | 417 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.443 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.476 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.617 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.443 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.443 |
LIG_SH3_3 | 636 | 642 | PF00018 | 0.446 |
LIG_SH3_4 | 479 | 486 | PF00018 | 0.443 |
LIG_SUMO_SIM_par_1 | 115 | 124 | PF11976 | 0.260 |
LIG_TRAF2_1 | 470 | 473 | PF00917 | 0.443 |
LIG_TYR_ITAM | 579 | 598 | PF00017 | 0.443 |
LIG_UBA3_1 | 585 | 590 | PF00899 | 0.443 |
LIG_UBA3_1 | 84 | 88 | PF00899 | 0.362 |
MOD_CDK_SPK_2 | 478 | 483 | PF00069 | 0.443 |
MOD_CDK_SPxxK_3 | 478 | 485 | PF00069 | 0.443 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.297 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.485 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.443 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.443 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.441 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.542 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.623 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.343 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.495 |
MOD_CK2_1 | 617 | 623 | PF00069 | 0.280 |
MOD_CMANNOS | 455 | 458 | PF00535 | 0.443 |
MOD_Cter_Amidation | 575 | 578 | PF01082 | 0.418 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.443 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.443 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.506 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.379 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.487 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.508 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.467 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.307 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.446 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.393 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.511 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.311 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.424 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.351 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.485 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.562 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.443 |
MOD_N-GLC_1 | 556 | 561 | PF02516 | 0.379 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.260 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.406 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.339 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.575 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.339 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.462 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.443 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.521 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.443 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.359 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.547 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.542 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.456 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.443 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.379 |
MOD_Plk_1 | 614 | 620 | PF00069 | 0.493 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.331 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.249 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.368 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.519 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.443 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.443 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.443 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.443 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.443 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.493 |
MOD_SUMO_for_1 | 162 | 165 | PF00179 | 0.315 |
MOD_SUMO_for_1 | 530 | 533 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 224 | 232 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 296 | 301 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 336 | 343 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 608 | 618 | PF00179 | 0.443 |
TRG_DiLeu_BaEn_1 | 113 | 118 | PF01217 | 0.381 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.311 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 312 | 315 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 449 | 452 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y6 | Leptomonas seymouri | 76% | 100% |
A0A0N1PC88 | Leptomonas seymouri | 27% | 91% |
A0A0S4J0Y2 | Bodo saltans | 28% | 74% |
A0A0S4JSQ6 | Bodo saltans | 52% | 100% |
A0A1X0ND08 | Trypanosomatidae | 27% | 91% |
A0A1X0NR71 | Trypanosomatidae | 63% | 100% |
A0A3Q8IGF4 | Leishmania donovani | 86% | 100% |
A0A3Q8IGS6 | Leishmania donovani | 26% | 91% |
A0A3R7LYC7 | Trypanosoma rangeli | 60% | 100% |
A4I1T8 | Leishmania infantum | 27% | 91% |
A4I2Z3 | Leishmania infantum | 86% | 100% |
C9ZJE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9AXX3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 91% |
E9AZ89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
O60993 | Crithidia fasciculata | 77% | 100% |
P0AES0 | Escherichia coli (strain K12) | 34% | 100% |
P0AES1 | Shigella flexneri | 34% | 100% |
P90518 | Crithidia fasciculata | 26% | 91% |
Q711P7 | Leishmania major | 85% | 100% |
Q9GT49 | Trypanosoma cruzi (strain CL Brener) | 59% | 100% |
V5ASH7 | Trypanosoma cruzi | 28% | 91% |
V5AYP7 | Trypanosoma cruzi | 59% | 100% |