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 |
Related structures:
AlphaFold database: A0A3S7WQU3
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0008270 | zinc ion binding | 6 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0046914 | transition metal ion binding | 5 | 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 | 108 | 112 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.446 |
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.532 |
CLV_MEL_PAP_1 | 330 | 336 | PF00089 | 0.680 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.683 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.661 |
DEG_SCF_TRCP1_1 | 243 | 249 | PF00400 | 0.439 |
DEG_SPOP_SBC_1 | 349 | 353 | PF00917 | 0.477 |
DOC_ANK_TNKS_1 | 294 | 301 | PF00023 | 0.510 |
DOC_ANK_TNKS_1 | 365 | 372 | PF00023 | 0.478 |
DOC_CDC14_PxL_1 | 198 | 206 | PF14671 | 0.569 |
DOC_CYCLIN_yCln2_LP_2 | 200 | 203 | PF00134 | 0.535 |
DOC_CYCLIN_yCln2_LP_2 | 204 | 210 | PF00134 | 0.494 |
DOC_MAPK_gen_1 | 332 | 339 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 77 | 87 | PF00069 | 0.657 |
DOC_MAPK_MEF2A_6 | 154 | 162 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 80 | 89 | PF00069 | 0.556 |
DOC_PP2B_LxvP_1 | 200 | 203 | PF13499 | 0.518 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.734 |
DOC_PP2B_LxvP_1 | 60 | 63 | PF13499 | 0.757 |
DOC_PP4_FxxP_1 | 16 | 19 | PF00568 | 0.723 |
DOC_PP4_FxxP_1 | 99 | 102 | PF00568 | 0.598 |
DOC_SPAK_OSR1_1 | 333 | 337 | PF12202 | 0.492 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.834 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 341 | 346 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 7 | 12 | PF00244 | 0.796 |
LIG_APCC_ABBA_1 | 160 | 165 | PF00400 | 0.519 |
LIG_BIR_III_4 | 111 | 115 | PF00653 | 0.574 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.424 |
LIG_eIF4E_1 | 276 | 282 | PF01652 | 0.479 |
LIG_EVH1_1 | 201 | 205 | PF00568 | 0.560 |
LIG_EVH1_1 | 60 | 64 | PF00568 | 0.715 |
LIG_EVH1_2 | 12 | 16 | PF00568 | 0.665 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.500 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.448 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.450 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.509 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.479 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.526 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.435 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.483 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.510 |
LIG_GBD_Chelix_1 | 24 | 32 | PF00786 | 0.477 |
LIG_LIR_Apic_2 | 14 | 19 | PF02991 | 0.726 |
LIG_LIR_Apic_2 | 165 | 170 | PF02991 | 0.525 |
LIG_LIR_Apic_2 | 342 | 346 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 267 | 277 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.444 |
LIG_LYPXL_yS_3 | 309 | 312 | PF13949 | 0.493 |
LIG_MLH1_MIPbox_1 | 91 | 95 | PF16413 | 0.424 |
LIG_MYND_1 | 199 | 203 | PF01753 | 0.499 |
LIG_PCNA_yPIPBox_3 | 324 | 333 | PF02747 | 0.460 |
LIG_Pex14_1 | 219 | 223 | PF04695 | 0.438 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.502 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.432 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.594 |
LIG_PTAP_UEV_1 | 345 | 350 | PF05743 | 0.462 |
LIG_PTB_Apo_2 | 263 | 270 | PF02174 | 0.503 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.506 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 343 | 347 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 152 | 156 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 81 | 85 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.341 |
LIG_SH2_STAT3 | 321 | 324 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.414 |
LIG_SH3_1 | 343 | 349 | PF00018 | 0.466 |
LIG_SH3_2 | 2 | 7 | PF14604 | 0.678 |
LIG_SH3_2 | 310 | 315 | PF14604 | 0.465 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.746 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.451 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.540 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.471 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.451 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.767 |
LIG_SUMO_SIM_anti_2 | 322 | 329 | PF11976 | 0.450 |
LIG_TRAF2_1 | 433 | 436 | PF00917 | 0.473 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.782 |
LIG_UBA3_1 | 280 | 289 | PF00899 | 0.441 |
LIG_WW_2 | 202 | 205 | PF00397 | 0.558 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.517 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.708 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.477 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.541 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.835 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.579 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.742 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.778 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.752 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.722 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.614 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.537 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.580 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.494 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.401 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.475 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.757 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.783 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.760 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.525 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.573 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.478 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.408 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.502 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.500 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.775 |
MOD_Plk_2-3 | 431 | 437 | PF00069 | 0.536 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.730 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.454 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.524 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.410 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.490 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.722 |
MOD_SUMO_for_1 | 367 | 370 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 118 | 125 | PF00179 | 0.483 |
TRG_DiLeu_BaEn_1 | 275 | 280 | PF01217 | 0.442 |
TRG_DiLeu_BaEn_2 | 29 | 35 | PF01217 | 0.722 |
TRG_DiLeu_BaLyEn_6 | 196 | 201 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 140 | 145 | PF00026 | 0.678 |
TRG_PTS1 | 436 | 439 | PF00515 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P570 | Leptomonas seymouri | 43% | 100% |
A0A0S4JNP6 | Bodo saltans | 22% | 100% |
A4H5V1 | Leishmania braziliensis | 65% | 99% |
A4HU45 | Leishmania infantum | 99% | 100% |
E9AMX4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QHQ2 | Leishmania major | 91% | 100% |