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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7XAI5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004518 | nuclease activity | 4 | 11 |
GO:0004519 | endonuclease activity | 5 | 11 |
GO:0004521 | RNA endonuclease activity | 5 | 11 |
GO:0004525 | ribonuclease III activity | 6 | 11 |
GO:0004540 | RNA nuclease activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 11 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 11 |
GO:0032296 | double-stranded RNA-specific ribonuclease activity | 5 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.414 |
CLV_MEL_PAP_1 | 561 | 567 | PF00089 | 0.574 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.788 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.723 |
CLV_PCSK_FUR_1 | 226 | 230 | PF00082 | 0.424 |
CLV_PCSK_FUR_1 | 526 | 530 | PF00082 | 0.604 |
CLV_PCSK_FUR_1 | 86 | 90 | PF00082 | 0.795 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.737 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.614 |
CLV_Separin_Metazoa | 186 | 190 | PF03568 | 0.394 |
CLV_Separin_Metazoa | 568 | 572 | PF03568 | 0.728 |
DEG_APCC_DBOX_1 | 227 | 235 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 503 | 511 | PF00400 | 0.691 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.719 |
DEG_SPOP_SBC_1 | 139 | 143 | PF00917 | 0.529 |
DOC_CDC14_PxL_1 | 212 | 220 | PF14671 | 0.434 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.732 |
DOC_CKS1_1 | 66 | 71 | PF01111 | 0.706 |
DOC_CYCLIN_yClb1_LxF_4 | 404 | 410 | PF00134 | 0.511 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.579 |
DOC_MAPK_gen_1 | 226 | 236 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 400 | 409 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 518 | 525 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 7 | 16 | PF00069 | 0.729 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 180 | 187 | PF00069 | 0.383 |
DOC_MAPK_MEF2A_6 | 518 | 527 | PF00069 | 0.644 |
DOC_MAPK_MEF2A_6 | 7 | 16 | PF00069 | 0.645 |
DOC_MAPK_NFAT4_5 | 180 | 188 | PF00069 | 0.383 |
DOC_MAPK_NFAT4_5 | 7 | 15 | PF00069 | 0.647 |
DOC_PP1_RVXF_1 | 263 | 269 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.767 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.682 |
DOC_PP2B_LxvP_1 | 572 | 575 | PF13499 | 0.615 |
DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.708 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.705 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.638 |
LIG_14-3-3_CanoR_1 | 205 | 212 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 571 | 575 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.729 |
LIG_Actin_WH2_2 | 457 | 474 | PF00022 | 0.521 |
LIG_APCC_ABBA_1 | 147 | 152 | PF00400 | 0.390 |
LIG_BIR_III_4 | 75 | 79 | PF00653 | 0.633 |
LIG_BRCT_BRCA1_1 | 259 | 263 | PF00533 | 0.439 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.532 |
LIG_DLG_GKlike_1 | 423 | 431 | PF00625 | 0.684 |
LIG_eIF4E_1 | 369 | 375 | PF01652 | 0.557 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.623 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.453 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.649 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.599 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.650 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.587 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.715 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.418 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.525 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.722 |
LIG_FXI_DFP_1 | 150 | 154 | PF00024 | 0.408 |
LIG_GBD_Chelix_1 | 336 | 344 | PF00786 | 0.351 |
LIG_Integrin_RGD_1 | 433 | 435 | PF01839 | 0.682 |
LIG_Integrin_RGDW_4 | 433 | 436 | PF00362 | 0.686 |
LIG_LIR_Apic_2 | 440 | 446 | PF02991 | 0.683 |
LIG_LIR_Apic_2 | 448 | 452 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 121 | 129 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 143 | 153 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 200 | 211 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 260 | 269 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 298 | 304 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 338 | 348 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 482 | 493 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 121 | 125 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 482 | 488 | PF02991 | 0.592 |
LIG_NRBOX | 229 | 235 | PF00104 | 0.397 |
LIG_PCNA_yPIPBox_3 | 392 | 402 | PF02747 | 0.513 |
LIG_PDZ_Class_3 | 582 | 587 | PF00595 | 0.574 |
LIG_Pex14_2 | 118 | 122 | PF04695 | 0.635 |
LIG_Pex14_2 | 146 | 150 | PF04695 | 0.387 |
LIG_PTB_Apo_2 | 159 | 166 | PF02174 | 0.400 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.741 |
LIG_SH2_CRK | 449 | 453 | PF00017 | 0.714 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.699 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.707 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.542 |
LIG_SH2_STAP1 | 380 | 384 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.524 |
LIG_SH3_1 | 449 | 455 | PF00018 | 0.658 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.650 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.587 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.720 |
LIG_SUMO_SIM_anti_2 | 505 | 511 | PF11976 | 0.691 |
LIG_SUMO_SIM_anti_2 | 68 | 75 | PF11976 | 0.623 |
LIG_SUMO_SIM_par_1 | 135 | 143 | PF11976 | 0.587 |
LIG_UBA3_1 | 230 | 238 | PF00899 | 0.404 |
LIG_WRC_WIRS_1 | 244 | 249 | PF05994 | 0.539 |
LIG_WRC_WIRS_1 | 485 | 490 | PF05994 | 0.513 |
MOD_CDK_SPK_2 | 322 | 327 | PF00069 | 0.474 |
MOD_CDK_SPK_2 | 559 | 564 | PF00069 | 0.674 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.644 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.464 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.657 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.432 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.687 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.489 |
MOD_Cter_Amidation | 56 | 59 | PF01082 | 0.749 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.631 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.565 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.665 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.640 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.704 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.660 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.510 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.558 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.739 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.417 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.707 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.664 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.689 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.663 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.658 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.410 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.609 |
MOD_N-GLC_2 | 2 | 4 | PF02516 | 0.639 |
MOD_N-GLC_2 | 207 | 209 | PF02516 | 0.555 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.565 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.542 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.624 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.678 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.678 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.714 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.730 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.620 |
MOD_NEK2_2 | 295 | 300 | PF00069 | 0.575 |
MOD_NEK2_2 | 412 | 417 | PF00069 | 0.455 |
MOD_NEK2_2 | 521 | 526 | PF00069 | 0.648 |
MOD_NEK2_2 | 534 | 539 | PF00069 | 0.577 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.554 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.711 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.719 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.678 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.414 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.572 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.523 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.715 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.390 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.523 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.349 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.661 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.634 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.617 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.711 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.424 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.480 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.602 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.636 |
MOD_SUMO_for_1 | 577 | 580 | PF00179 | 0.681 |
TRG_AP2beta_CARGO_1 | 148 | 157 | PF09066 | 0.410 |
TRG_DiLeu_BaEn_1 | 95 | 100 | PF01217 | 0.700 |
TRG_DiLeu_BaEn_2 | 263 | 269 | PF01217 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 226 | 231 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 94 | 99 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.587 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.699 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 226 | 229 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.790 |
TRG_ER_diArg_1 | 517 | 519 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 525 | 528 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 85 | 88 | PF00400 | 0.733 |
TRG_NLS_Bipartite_1 | 144 | 160 | PF00514 | 0.404 |
TRG_NLS_MonoExtN_4 | 226 | 231 | PF00514 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3V7 | Leptomonas seymouri | 47% | 99% |
A0A1X0P9H0 | Trypanosomatidae | 47% | 100% |
A0A3R7KSN8 | Trypanosoma rangeli | 46% | 100% |
A4HNW5 | Leishmania braziliensis | 77% | 100% |
A4ICM9 | Leishmania infantum | 100% | 100% |
D0A2T3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ASM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q6T449 | Leishmania major | 92% | 100% |
V5BZU7 | Trypanosoma cruzi | 46% | 100% |