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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HJ79
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.373 |
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.614 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.778 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.710 |
CLV_PCSK_FUR_1 | 163 | 167 | PF00082 | 0.556 |
CLV_PCSK_FUR_1 | 277 | 281 | PF00082 | 0.654 |
CLV_PCSK_FUR_1 | 332 | 336 | PF00082 | 0.803 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.603 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.722 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.677 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.786 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.595 |
CLV_PCSK_PC7_1 | 275 | 281 | PF00082 | 0.806 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.651 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.644 |
DOC_ANK_TNKS_1 | 218 | 225 | PF00023 | 0.538 |
DOC_CYCLIN_RxL_1 | 111 | 120 | PF00134 | 0.601 |
DOC_MAPK_gen_1 | 161 | 169 | PF00069 | 0.698 |
DOC_MAPK_MEF2A_6 | 163 | 171 | PF00069 | 0.690 |
DOC_MAPK_RevD_3 | 365 | 380 | PF00069 | 0.554 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.564 |
DOC_USP7_UBL2_3 | 168 | 172 | PF12436 | 0.745 |
DOC_USP7_UBL2_3 | 184 | 188 | PF12436 | 0.613 |
DOC_USP7_UBL2_3 | 207 | 211 | PF12436 | 0.539 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.684 |
LIG_14-3-3_CanoR_1 | 277 | 287 | PF00244 | 0.783 |
LIG_14-3-3_CanoR_1 | 362 | 370 | PF00244 | 0.801 |
LIG_14-3-3_CanoR_1 | 99 | 106 | PF00244 | 0.496 |
LIG_Actin_WH2_2 | 69 | 86 | PF00022 | 0.588 |
LIG_APCC_ABBAyCdc20_2 | 172 | 178 | PF00400 | 0.550 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_1 | 201 | 205 | PF00533 | 0.538 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.621 |
LIG_BRCT_BRCA1_2 | 201 | 207 | PF00533 | 0.539 |
LIG_Clathr_ClatBox_1 | 367 | 371 | PF01394 | 0.586 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.570 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.501 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.558 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.784 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.521 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.723 |
LIG_LIR_Gen_1 | 323 | 330 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 413 | 420 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 323 | 329 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 413 | 418 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.614 |
LIG_PDZ_Class_2 | 415 | 420 | PF00595 | 0.776 |
LIG_SH2_CRK | 326 | 330 | PF00017 | 0.558 |
LIG_SH2_GRB2like | 94 | 97 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 326 | 330 | PF00017 | 0.558 |
LIG_SH2_PTP2 | 415 | 418 | PF00017 | 0.520 |
LIG_SH2_SRC | 94 | 97 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.520 |
LIG_SH3_2 | 270 | 275 | PF14604 | 0.808 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.537 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.797 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.564 |
LIG_UBA3_1 | 367 | 375 | PF00899 | 0.549 |
LIG_WRPW_2 | 57 | 60 | PF00400 | 0.371 |
MOD_CDK_SPK_2 | 183 | 188 | PF00069 | 0.560 |
MOD_CDK_SPK_2 | 335 | 340 | PF00069 | 0.684 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.573 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.649 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.485 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.526 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.618 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.514 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.724 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.598 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.729 |
MOD_Cter_Amidation | 277 | 280 | PF01082 | 0.765 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.599 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.504 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.556 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.787 |
MOD_GlcNHglycan | 236 | 240 | PF01048 | 0.687 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.733 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.559 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.553 |
MOD_GlcNHglycan | 320 | 325 | PF01048 | 0.562 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.531 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.504 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.787 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.486 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.591 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.573 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.588 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.559 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.625 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.564 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.564 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.551 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.649 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.810 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.584 |
MOD_NEK2_2 | 199 | 204 | PF00069 | 0.535 |
MOD_NEK2_2 | 36 | 41 | PF00069 | 0.601 |
MOD_NEK2_2 | 94 | 99 | PF00069 | 0.401 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.810 |
MOD_PK_1 | 99 | 105 | PF00069 | 0.493 |
MOD_PKA_1 | 279 | 285 | PF00069 | 0.676 |
MOD_PKA_1 | 291 | 297 | PF00069 | 0.601 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.568 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.706 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.681 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.534 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.591 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.804 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.610 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.380 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.545 |
MOD_PKB_1 | 277 | 285 | PF00069 | 0.706 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.595 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.681 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.563 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.683 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.530 |
MOD_Plk_2-3 | 298 | 304 | PF00069 | 0.553 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.526 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.565 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.726 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.685 |
MOD_SUMO_for_1 | 147 | 150 | PF00179 | 0.571 |
MOD_SUMO_for_1 | 356 | 359 | PF00179 | 0.565 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.520 |
TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.729 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.823 |
TRG_NLS_Bipartite_1 | 192 | 214 | PF00514 | 0.794 |
TRG_NLS_MonoCore_2 | 331 | 336 | PF00514 | 0.586 |
TRG_NLS_MonoExtC_3 | 191 | 196 | PF00514 | 0.688 |
TRG_NLS_MonoExtC_3 | 209 | 214 | PF00514 | 0.755 |
TRG_NLS_MonoExtC_3 | 332 | 337 | PF00514 | 0.592 |
TRG_NLS_MonoExtC_3 | 377 | 382 | PF00514 | 0.565 |
TRG_NLS_MonoExtN_4 | 207 | 214 | PF00514 | 0.766 |
TRG_NLS_MonoExtN_4 | 330 | 337 | PF00514 | 0.589 |
TRG_NLS_MonoExtN_4 | 375 | 382 | PF00514 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.616 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIK0 | Leptomonas seymouri | 31% | 100% |
A0A3S7X4A5 | Leishmania donovani | 59% | 100% |
A4I6M3 | Leishmania infantum | 59% | 100% |
E9B1P6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
Q4Q6G4 | Leishmania major | 59% | 96% |